Botulinum toxin type A is a prescription medication administered through carefully targeted injections into specific muscles or treatment areas. It is used in both aesthetic and medical therapeutic medicine to temporarily reduce muscle activity or block certain nerve signals.

In aesthetic medicine, botulinum toxin type A is commonly used to temporarily soften the appearance of dynamic facial lines caused by repetitive muscle movement. Depending on the product used, FDA-approved cosmetic indications may include moderate to severe frown lines between the eyebrows, forehead lines, and crow’s feet in adults.

In medical therapeutic applications, botulinum toxin type A may be used to treat certain neuromuscular and glandular conditions. Depending on the formulation and indication, FDA-approved therapeutic uses may include chronic migraine, cervical dystonia, muscle spasticity, blepharospasm, overactive bladder, severe underarm sweating (hyperhidrosis), and other conditions involving excessive muscle contraction or nerve signaling. When used for hyperhidrosis, botulinum toxin type A temporarily blocks the nerve signals responsible for activating sweat glands in the treated area.

Additional cosmetic and therapeutic treatment areas may be recommended by your provider as “off-label” uses. Off-label use refers to treatments that are medically accepted, evidence-based, and commonly performed within clinical practice, but have not received specific FDA approval for that particular indication.

Botulinum toxin type A is administered through a series of small, targeted injections into specific muscles or treatment areas. In aesthetic treatments, the medication works by temporarily reducing muscle activity responsible for dynamic facial lines and expressions.

For the treatment of hyperhidrosis, small amounts of botulinum toxin type A may be injected superficially into areas such as the underarms, palms, or soles of the feet, to temporarily reduce sweat gland activity.

Results develop gradually over several days, with optimal cosmetic results typically seen around 14 days following treatment. FDA-approved cosmetic botulinum toxin treatments are generally recommended no more frequently than every 3–4 months, though duration and response may vary based on the treatment area, product used, dosage, metabolism, muscle activity, and individual lifestyle factors.

Because the effects of botulinum toxin type A are temporary, maintenance treatments are required to sustain desired results.

As with any injectable procedure, botulinum toxin type A treatments carry potential risks, side effects, complications, and variable outcomes. Common injection-related reactions you may experience include redness, swelling, bruising, tenderness, discomfort, pinpoint bleeding, or temporary headache at the injection site.

Additional reported side effects and complications may include, but are not limited to:

• Eyelid or eyebrow drooping (ptosis)
• Facial asymmetry or unintended muscle weakness
• Altered facial expression or facial tightness
• Dry eyes, excessive tearing, or eyelid swelling
• Blurred vision, double vision, or visual disturbances
• Dry mouth
• Neck pain or muscle soreness
• Fatigue or flu-like symptoms
• Nausea or dizziness
• Difficulty swallowing or speaking
• Allergic or hypersensitivity reactions
• Reduced effectiveness, shortened duration of response, or development of treatment resistance over time
• Rare spread of toxin effect causing generalized muscle weakness or breathing difficulties

In rare cases, the effects of botulinum toxin type A may spread beyond the injection site. You should seek immediate medical attention if you experience difficulty breathing, difficulty swallowing, vision changes, severe muscle weakness, loss of bladder control, or speech difficulties following treatment.

If you take medications or supplements that may increase bleeding or bruising — including aspirin, ibuprofen, naproxen, Advil®, Aleve®, Motrin®, prescription blood thinners, fish oil, vitamin E, or certain herbal supplements — you may have an increased risk of bruising. You should discuss all medications and supplements with your provider prior to treatment and should not discontinue prescribed medications without approval from your prescribing physician.

Botulinum toxin type A treatment may be contraindicated if you:

• Have myasthenia gravis (MG), Lambert-Eaton syndrome, amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), Guillain-Barré syndrome (GBS), or another significant neuromuscular disorder
• Have a known allergy or hypersensitivity to botulinum toxin products or their ingredients, including human albumin
  • Are pregnant, attempting to become pregnant, or breastfeeding
• Have an active infection, inflammation, or skin condition at the treatment site
• Are taking medications that interfere with neuromuscular transmission, including aminoglycoside antibiotics or similar agents

While many patients are pleased with their results, aesthetic and therapeutic outcomes vary between individuals. Your longevity of results, onset of effect, and degree of improvement cannot be predicted or guaranteed. No guarantees or warranties have been made regarding the effectiveness or duration of your treatment results. Desired outcomes may require maintenance treatments, treatment adjustments, combination therapies, or additional sessions at additional cost.

Botulinum toxin type A is widely used in aesthetic and therapeutic medicine and may provide temporary improvement in dynamic facial lines, certain patterns of muscle activity, and hyperhidrosis in treated areas. Individual response, longevity of results, and degree of improvement vary between patients. No specific outcome or degree of improvement can be guaranteed.

This treatment is elective and voluntary. You may choose to decline treatment at any time.

Alternative treatment options may include no treatment, skincare products, other botulinum toxin formulations, fillers, laser or energy-based treatments, microneedling, hyperhidrosis-specific therapies, surgical procedures, or other medical and aesthetic treatments. Each alternative carries its own risks, benefits, limitations, costs, and expected outcomes.

You may arrive to your appointment with or without cosmetics applied. The treatment area will be thoroughly cleansed and prepared prior to treatment. Cosmetics may be cautiously reapplied following treatment unless otherwise directed by your provider.

For the first 4-6 hours following treatment:

• Remain upright and avoid lying down or bending forward
• Avoid exercise
• Avoid touching, rubbing, or massaging treated areas
• Avoid hats or pressure on treated areas
• Avoid showering, hair washing, or blow-drying
• Avoid wearing glasses if bunny lines were treated

These precautions are intended to help reduce the risk of unintended product spread and undesired outcomes.

You may resume normal facial movement following treatment, unless otherwise directed by your provider. No specific facial exercises or repetitive muscle movements are required following botulinum toxin type A treatment.

Results develop gradually and are not immediate. Initial improvement may begin within several days following treatment, with peak cosmetic results typically seen around 14–21 days.

Please allow at least 14 days following treatment before evaluating your final cosmetic results or treatment response.

You should contact us at 231.598.8828 if you experience unexpected side effects, worsening pain, prolonged swelling, signs of infection, significant facial asymmetry, or other concerning symptoms following treatment.

Seek immediate medical attention or call 911 if you experience difficulty breathing, difficulty swallowing, chest pain, severe allergic reaction, vision loss, sudden vision changes, severe muscle weakness, or any symptoms you believe may represent a medical emergency.

Zepbound® is an FDA-approved prescription medication used for chronic weight management in adults adults 18 years of age and older with obesity or overweight with at least one weight-related medical condition, when used in combination with reduced calorie intake, lifestyle modification, and increased physical activity.

Zepbound® contains tirzepatide, a glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist. It works by helping regulate appetite, increasing feelings of fullness, slowing gastric emptying, and supporting metabolic regulation related to blood sugar and energy balance.

Medical weight management with Zepbound® is intended to be part of a comprehensive, medically supervised treatment plan that may include nutritional guidance, lifestyle modification, behavioral support, and ongoing clinical follow-up.

Results and response to treatment vary between individuals. No specific amount of weight loss or medical outcome can be guaranteed.

Zepbound® is administered as a once-weekly subcutaneous injection (under the skin) into the abdomen, thigh, or upper arm. Injections should be administered on the same day each week, with or without food, unless otherwise directed by your provider.

Treatment is typically started at a lower dose and gradually increased over time to help minimize gastrointestinal side effects and improve treatment tolerance. Injection sites should be rotated with each dose.

Regular follow-up appointments, monitoring, and adherence to your prescribed treatment plan are important for safe and effective treatment. Your provider may adjust your dosage, treatment schedule, or overall care plan based on your response, side effects, laboratory findings, medical history, and treatment goals.

As with any prescription medication, Zepbound® carries potential risks, side effects, complications, and variable outcomes.

Common side effects may include nausea, vomiting, diarrhea, constipation, abdominal pain or discomfort, indigestion, bloating, gas, heartburn, decreased appetite, fatigue, headache, dizziness, hair loss, and injection-site reactions.

Additional risks and complications may include severe gastrointestinal symptoms, delayed stomach emptying (gastroparesis), dehydration, gallbladder disease or gallstones, pancreatitis, kidney injury or worsening kidney function, low blood sugar (especially when used with insulin or other diabetes medications), allergic or hypersensitivity reactions including anaphylaxis and angioedema, intestinal obstruction or severe constipation, vision changes or worsening diabetic retinopathy in patients with type 2 diabetes, increased heart rate, suicidal thoughts or behaviors, and possible loss of lean muscle mass with rapid weight loss.

Zepbound® carries an FDA boxed warning regarding the potential risk of thyroid C-cell tumors observed in animal studies. It is unknown whether Zepbound® causes thyroid C-cell tumors, including medullary thyroid carcinoma (MTC), in humans.

Zepbound® should not be used if you have a personal or family history of medullary thyroid carcinoma (MTC), Multiple Endocrine Neoplasia syndrome type 2 (MEN 2), or a history of serious allergic reaction to tirzepatide or any component of the medication.

You should discuss treatment carefully with your provider if you have a history of pancreatitis, kidney disease, gallbladder disease, diabetes, severe gastrointestinal disease, gastroparesis, diabetic retinopathy, depression, suicidal thoughts, or other significant medical conditions. You should also discuss treatment with your provider if you are pregnant, planning pregnancy, breastfeeding, or planning surgery or procedures requiring anesthesia.

Zepbound® should not be used in combination with other tirzepatide-containing products or GLP-1 receptor agonist medications unless specifically directed by your prescribing medical provider.

You should fully disclose your medical history, medications, supplements, allergies, and changes in health status to your provider prior to treatment.

Potential benefits of treatment with Zepbound® may include weight loss, appetite reduction, improved portion control, increased feelings of fullness, and improvement in certain weight-related health conditions when used in combination with reduced calorie intake, lifestyle modification, and increased physical activity.

Results vary between individuals and are influenced by factors including medical history, metabolism, adherence to treatment, nutrition, physical activity, medication tolerance, and other lifestyle factors. No specific amount of weight loss, body composition change, or medical outcome can be guaranteed.

This treatment is elective and voluntary. You may choose to decline treatment or discontinue therapy at any time.

Alternative treatment options may include nutritional and lifestyle modification alone, behavioral counseling, medically supervised weight management programs, other FDA-approved weight-loss medications, bariatric surgery, or no treatment. Each alternative carries its own risks, benefits, limitations, costs, and expected outcomes.

Zepbound® is self-administered as a once-weekly subcutaneous injection (under the skin) into the abdomen, thigh, or upper arm. Injections should be administered on the same day each week, with or without food, unless otherwise directed by your provider.

Injection sites should be rotated with each dose to help minimize irritation. Do not inject into areas that are bruised, tender, scarred, irritated, or affected by skin conditions.

If you miss a dose, administer it as soon as possible within four (4) days of the missed dose. If more than four days have passed, skip the missed dose and resume your normal dosing schedule on your next scheduled injection day. Do not administer two doses within 72 hours of one another.

Do not share injection pens or supplies with other individuals. Used injection pens and needles should be disposed of in an appropriate sharps container according to local regulations and pharmacy guidance.

Prescription processing, refill timing, medication availability, and shipping timelines may vary and are outside the control of Embry & Co.

For questions regarding your prescription status, shipment, refills, pricing, or medication availability, please contact the pharmacy directly.

LillyDirect Pharmacy
844.559.3471
1555 S Harding St, Suite 171-B68
Indianapolis, IN 46221

If you have questions about your dosage, side effects, treatment plan, or overall care, please contact Embry & Co. at 231.598.8828.

Zepbound® is intended to be used in combination with reduced calorie intake, increased physical activity, and long-term lifestyle modification. Consistent nutrition, hydration, protein intake, sleep, resistance training, and regular physical activity may help support treatment success and preservation of lean muscle mass during weight loss.

For nutrition guidance and meal planning support, please review the Nutrition Guide

For local Pilates and movement support, Embry & Co. recommends
Pilates Big Rapids

For guided at-home Pilates and low-impact movement classes, Embry & Co. recommends
Move With Nicole

Results with Zepbound® develop gradually over time and vary between individuals. Some patients may begin noticing changes in appetite, portion control, cravings, energy balance, or weight within the first several weeks of treatment, while others may require additional time and dose adjustments.

Weight loss and metabolic response are influenced by multiple factors including medication adherence, nutrition, physical activity, sleep, medical history, dosing, lifestyle habits, and individual metabolism. Ongoing follow-up and long-term lifestyle modification are important components of treatment success.

No specific amount or rate of weight loss can be guaranteed. Weight regain may occur after dose reduction or discontinuation of treatment. Long-term maintenance may require continued medical management, nutritional support, physical activity, and ongoing lifestyle modification.

You should contact us at 231.598.8828 if you experience persistent nausea, vomiting, diarrhea, constipation, worsening abdominal discomfort, dehydration, injection-site reactions, medication intolerance, or difficulty obtaining your prescription after contacting your pharmacy.

Notify your provider promptly if you develop a new neck mass, persistent hoarseness, difficulty swallowing, or swelling in the neck area during treatment.

Seek immediate medical attention or call 911 if you experience severe abdominal pain that does not resolve, chest pain, difficulty breathing, severe allergic reaction, facial swelling, severe dehydration, vision changes, signs of pancreatitis, signs of gallbladder complications, suicidal thoughts or behaviors, or any symptoms you believe may represent a medical emergency.

For the purposes of this treatment information and documentation, the term “filler” refers to hyaluronic acid (HA)-based dermal filler products, including the RHA® Collection by Revance Aesthetics and Teoxane, used for facial balancing, contouring, structural support, soft tissue enhancement, and correction of facial wrinkles and folds.

The RHA® Collection is an FDA-approved line of hyaluronic acid fillers designed to adapt to dynamic facial movement for natural-looking results at rest and in motion. Hyaluronic acid is a naturally occurring substance found within the skin and soft tissues that helps support hydration, flexibility, and volume.

FDA-approved indications for hyaluronic acid fillers include:

• Correction of moderate to severe facial wrinkles and folds, including nasolabial folds.
• Correction of dynamic facial wrinkles and folds associated with facial movement.
• Correction of moderate to severe perioral rhytids (lip lines).
• Lip augmentation and improvement of lip fullness.
• Cheek augmentation.
• Correction of age-related midface contour deficiencies.
• Soft tissue augmentation and facial volume restoration.

Additional treatment areas, facial balancing approaches, injection techniques, and aesthetic indications may be considered off-label uses and are performed at the discretion of your provider based on clinical judgment, facial anatomy, and individual treatment goals.

Filler treatments are performed through a series of injections placed within targeted areas of the face or soft tissues to support facial balancing, contouring, volume restoration, structural support, or enhancement.

Depending on the treatment area, your provider may use a needle, microcannula, or combination technique during treatment. A topical anesthetic, local anesthetic, dental block, or ice may be used to improve comfort prior to or during the procedure.

Treatment technique, product selection, injection depth, placement, and volume vary based on facial anatomy, tissue characteristics, treatment goals, provider assessment, and individual response to treatment.

Temporary redness, swelling, bruising, tenderness, asymmetry, firmness, or injection-site discomfort are common following treatment. Multiple treatments or maintenance treatments may be recommended to help achieve or maintain desired results.

As with any aesthetic procedure, filler treatment carries potential risks, side effects, complications, and variable outcomes.

Common treatment responses may include: redness, swelling, bruising, tenderness, firmness, itching, asymmetry, lumpiness, temporary discomfort, injection-site reactions, or sensitivity within the treatment area.

Additional risks and complications may include: allergic or hypersensitivity reactions, prolonged swelling, delayed healing, infection, activation of herpes simplex virus (cold sores), migration of filler product, visible or palpable filler, granuloma formation, scarring, dissatisfaction with cosmetic outcome, or the need for additional treatment or correction.

Although uncommon, serious complications may occur, including vascular occlusion, tissue ischemia, skin necrosis, stroke, or blindness if filler is unintentionally injected into or around a blood vessel. Some complications may be temporary or permanent despite treatment. Immediate recognition and treatment of vascular complications are critical but may not prevent permanent injury.

Hyaluronic acid fillers may be dissolved with hyaluronidase (including Hylenex® or similar products) if medically appropriate or clinically indicated; however, correction or reversal may not fully restore the original appearance or eliminate all complications.

Treatment may not be appropriate if you:

• Are pregnant or breastfeeding.
• Have active infection, cold sores, rash, or inflammation within or near the treatment area.
• Have known allergies or hypersensitivity to filler ingredients or lidocaine-containing products.
• Have a bleeding disorder or use medications or supplements that may increase bleeding or bruising
• Have a history of severe allergic reactions or anaphylaxis.
• Have autoimmune disease, immunosuppressive conditions, or medical conditions that may impair healing.

Hyaluronidase (including Hylenex® or similar products) is an enzyme that may be used to dissolve hyaluronic acid filler if medically necessary or clinically indicated. Hyaluronidase may be recommended to help treat complications including vascular occlusion, prolonged swelling, asymmetry, overcorrection, misplaced filler, nodules, or unsatisfactory cosmetic outcome.

Use of hyaluronidase for cosmetic filler reversal or management of filler-related complications is considered an off-label use commonly performed within aesthetic medicine.

Potential risks and side effects of hyaluronidase may include redness, swelling, bruising, itching, allergic reaction, incomplete correction, undesired cosmetic changes, or degradation of both injected filler and naturally occurring hyaluronic acid within the treatment area.

Patients with a history of significant allergies, prior reaction to hyaluronidase products, bee or wasp sting allergy, or multiple severe allergies should notify their provider prior to treatment.

The safety of hyaluronidase during pregnancy or breastfeeding has not been fully established.

Multiple treatment sessions or repeated dosing may be necessary depending on the complication being treated and individual response.

In the event vascular compromise or another serious filler-related complication is suspected, your provider may recommend immediate administration of hyaluronidase in an attempt to reduce the risk of tissue injury or permanent complications. Despite prompt recognition and treatment, permanent injury may still occur.

Potential benefits of filler treatment may include: facial balancing, soft tissue enhancement, structural support, restoration of age-related volume loss, contour improvement, lip enhancement, improvement in the appearance of facial wrinkles and folds, and overall facial rejuvenation.

Results vary between individuals and are influenced by factors, including: facial anatomy, metabolism, product selection, treatment area, lifestyle factors, injection technique, and individual response to treatment. No specific cosmetic result, degree of correction, symmetry, or longevity of results can be guaranteed.

This treatment is elective and voluntary. You may choose to decline treatment at any time.

Alternative treatment options may include no treatment, skincare products, neuromodulators, biostimulatory injectables, laser procedures, microneedling, surgical procedures, fat transfer, or other medical and aesthetic treatments. Each alternative carries its own risks, benefits, limitations, costs, and expected outcomes.

Avoid dental procedures, dental cleanings, or other elective dental treatment within 14 days of filler treatment around the mouth, unless otherwise discussed with your provider.

To reduce bruising and downtime following filler treatment, avoid NSAIDs (e.g., ibuprofen), fish oil, vitamin E, alcohol, or other medications and supplements that may increase bleeding or bruising 7 days prior to treatment, unless medically necessary or otherwise directed by your prescribing physician.

Do not discontinue prescription medications without first consulting with your prescribing medical provider.

You may arrive to your appointment with or without cosmetics applied. The treatment area will be thoroughly cleansed and prepared prior to treatment. Cosmetics may be cautiously reapplied following treatment unless otherwise directed by your provider.

Cold compresses may be applied intermittently for comfort, swelling, or tenderness, as needed. Some patients choose to use Arnica topically or orally as an off-label supportive option intended to help minimize bruising and swelling.

If discomfort occurs following treatment, acetaminophen (Tylenol®) is commonly preferred over NSAIDs such as ibuprofen, naproxen, aspirin, or Advil® when appropriate, as NSAIDs may increase bruising or bleeding risk. Consult with your medical provider regarding medication safety and potential interactions.

Avoid dental procedures, dental cleanings, or other elective dental treatment within 14 days of filler treatment around the mouth unless otherwise discussed with your provider.

Filler undergoes gradual tissue integration following treatment. While initial improvement is visible immediately, final settling and tissue integration may take approximately 4–8 weeks depending on the treatment area, product used, metabolism, swelling response, and individual healing characteristics.

Healing response and downtime vary between individuals and treatment areas. Final results may not be fully visible until swelling has resolved and tissue integration has occurred.

You should contact us at 231.598.8828 if you experience worsening redness, prolonged swelling, increasing pain, excessive bruising, firmness, blanching or discoloration of the skin, delayed healing, signs of infection, cold sore outbreak, worsening lumpiness, or other concerning symptoms following treatment.

Seek immediate medical attention or call 911 if you experience severe pain, vision changes, vision loss, difficulty breathing, chest pain, severe allergic reaction, facial weakness, sudden numbness, difficulty speaking, confusion, severe headache, dizziness, difficulty walking, loss of coordination, or other stroke-like symptoms following treatment.

Hydroquinone is a topical prescription skin-lightening medication commonly used to improve the appearance of hyperpigmentation, melasma, post-inflammatory pigmentation, sun damage, and uneven skin tone by reducing excess pigment production within the skin.

Hydroquinone may be prescribed alone or incorporated into a broader skincare regimen alongside retinoids, antioxidants, exfoliants, chemical peels, lasers, microneedling, or other aesthetic treatments depending on treatment goals and provider assessment.

Results develop gradually over time and require consistent use, sun protection, and adherence to treatment instructions. Hydroquinone is typically used for limited treatment durations unless otherwise directed by your provider.

Additional uses, treatment combinations, strengths, and treatment areas may be considered off-label and are performed at the discretion of your provider based on clinical judgment, skin condition, and individual treatment goals.

Hydroquinone is applied topically to areas of unwanted pigmentation or uneven skin tone as directed by your provider. Frequency of use, treatment duration, concentration, and accompanying skincare products vary based on skin condition, treatment goals, tolerance, and provider assessment.

Depending on your treatment plan, hydroquinone may be used alone or in combination with other prescription or non-prescription skincare products and aesthetic procedures.

Because hydroquinone may increase skin sensitivity, gradual introduction and adjustment of use may be recommended to help minimize irritation.

Periodic follow-up appointments and skin evaluations are recommended to monitor treatment response, assess skin tolerance, adjust treatment plans when appropriate, and help reduce the risk of complications associated with prolonged use.

As with any prescription skincare treatment, hydroquinone carries potential risks, side effects, complications, and variable outcomes.

Common treatment responses may include: dryness, peeling, redness, irritation, burning, itching, sensitivity, temporary inflammation, or increased sun sensitivity.

Additional risks and complications may include: allergic reaction, persistent irritation, rebound pigmentation, uneven pigment lightening, post-inflammatory pigmentation, worsening discoloration, or dissatisfaction with cosmetic outcome.

Although uncommon, prolonged or inappropriate use of hydroquinone may increase the risk of exogenous ochronosis, a rare condition involving blue-black or gray discoloration of the skin.

Treatment may not be appropriate if you:

• Are pregnant or breastfeeding.
• Have known allergy or hypersensitivity to hydroquinone or treatment components.
• Have severely irritated, inflamed, sunburned, or compromised skin within the treatment area.
• Are unable or unwilling to consistently use sun protection.

Hydroquinone may increase skin sensitivity and may not be tolerated by all individuals.

Potential benefits of hydroquinone treatment may include: improvement in hyperpigmentation, melasma, post-inflammatory pigmentation, uneven skin tone, sun damage, and overall skin clarity.

Results vary between individuals and are influenced by skin condition, depth of pigmentation, consistency of use, sun exposure, treatment adherence, skincare regimen, lifestyle factors, and individual response to treatment. No specific cosmetic result or degree of pigment correction can be guaranteed.

This treatment is elective and voluntary. You may choose to decline treatment at any time.

Alternative treatment options may include no treatment, retinoids, vitamin C, azelaic acid, kojic acid, cysteamine, chemical peels, laser procedures, microneedling, prescription skincare products, or other medical and aesthetic treatments. Each alternative carries its own risks, benefits, limitations, costs, and expected outcomes.

Mild dryness, peeling, redness, irritation, or sensitivity may occur during treatment. Gradual introduction or adjustment of use may be recommended depending on skin tolerance.

Use only products recommended or approved by your provider while using hydroquinone.

Consistent daily sunscreen use is essential during treatment.

Hydroquinone works gradually over time by reducing the appearance of excess pigmentation and uneven skin tone. Improvement commonly develops over several weeks to months depending on the depth and severity of pigmentation, treatment consistency, sun exposure, skincare regimen, and individual response to treatment.

Consistent use and daily sunscreen application are important to help support treatment success and maintenance of results. Some patients may require combination therapy, maintenance treatment, or periodic treatment breaks, as directed by their provider.

Results vary between individuals, and recurrence of pigmentation may occur, particularly with continued sun exposure, hormonal influences, inflammation, or interruption of treatment.

No specific cosmetic result or degree of pigment correction can be guaranteed.

You should contact us at 231.598.8828 if irritation or discomfort occurs to discuss possible treatment adjustment or product modification prior to discontinuing treatment, unless a severe reaction develops.

You should also contact us at 231.598.8828 if you experience worsening irritation, persistent redness, excessive dryness, blistering, significant peeling, worsening pigmentation, uneven lightening of the skin, allergic reaction, or other concerning symptoms during treatment.

Seek immediate medical attention or call 911 if you experience difficulty breathing, facial swelling, severe allergic reaction, chest pain, or any symptoms you believe may represent a medical emergency.

Facials are non-invasive aesthetic skin treatments designed to support overall skin health, hydration, exfoliation, skin clarity, and maintenance of the skin barrier. Treatment techniques, products, and treatment steps vary depending on skin condition, treatment goals, provider assessment, and the facial selected.

Facials may incorporate cleansing, exfoliation, extractions, hydration, massage, dermaplaning, enzymes, masks, and customized medical-grade skincare protocols depending on treatment selection and provider discretion.

Facials may be performed alone or incorporated into broader skincare and aesthetic treatment plans alongside prescription skincare products and procedures.

Additional treatment techniques, combinations, and protocols may be considered off-label and are performed at the discretion of your provider based on clinical judgment, skin condition, and individual treatment goals.

Facials involve a customized combination of skincare products, exfoliation methods, treatment techniques, and supportive modalities selected based on skin condition, treatment goals, and provider assessment.

Some facials may include mild exfoliation, dermaplaning, extractions, enzymes, acids, or advanced skincare products.

Treatment frequency and maintenance recommendations vary depending on skin condition, skincare regimen, treatment goals, and individual response.

As with any aesthetic skin treatment, facials carry potential risks, side effects, complications, and variable outcomes.

Common treatment responses may include: temporary redness, dryness, sensitivity, tightness, mild irritation, temporary breakouts, tenderness, or sensitivity to skincare products.

Additional risks and complications may include: allergic reaction, irritation, infection, post-inflammatory pigmentation, delayed healing, worsening acne, skin sensitivity, dissatisfaction with cosmetic outcome, or the need for additional treatment.

Treatment may not be appropriate if you:

• Have active infection, open wounds, rash, severe inflammation, sunburn, or irritation within the treatment area.
• Have known allergy or hypersensitivity to treatment products or ingredients.
• Have recently undergone aggressive exfoliation, laser procedures, or other treatments that may compromise the skin barrier.
• Are using medications or prescription skincare products that may increase skin sensitivity.

You should fully disclose your medical history, medications, allergies, recent procedures, pregnancy status, breastfeeding status, and changes in health status to your provider prior to treatment.

Potential benefits of facials may include: improvement in hydration, skin texture, smoothness, brightness, congestion, skin clarity, exfoliation, relaxation, and overall skin health.

Results vary between individuals and are influenced by skin condition, skincare regimen, lifestyle factors, treatment consistency, home care compliance, and individual response to treatment. No specific cosmetic result or degree of improvement can be guaranteed.

This treatment is elective and voluntary. You may choose to decline treatment at any time.

Alternative treatment options may include no treatment, prescription skincare products, chemical peels, dermaplaning, microneedling, laser procedures, hydrafacial treatments, or other medical and aesthetic treatments. Each alternative carries its own risks, benefits, limitations, costs, and expected outcomes.

You may arrive to your appointment with or without cosmetics applied. The treatment area will be thoroughly cleansed and prepared prior to treatment.

Please remove waterproof cosmetics prior to your visit when possible.

Mild redness, dryness, sensitivity, tightness, or temporary irritation may occur following treatment depending on the facial selected and individual skin response.

Use only products recommended or approved by your provider if irritation or sensitivity occurs following treatment.

Avoid aggressive exfoliation, excessive heat exposure, or potentially irritating skincare products immediately following treatment unless otherwise directed by your provider.

Consistent sunscreen use is recommended following treatment.

Facials are intended to support overall skin health, maintenance, hydration, exfoliation, and skin quality over time. Some patients notice improvement in brightness, smoothness, hydration, congestion, or overall skin appearance following a single treatment, while others may benefit from ongoing maintenance treatments and consistent home skincare.

Results vary between individuals and are influenced by treatment consistency, skincare compliance, skin condition, lifestyle factors, sun exposure, and overall skin health.

No specific cosmetic result or degree of improvement can be guaranteed.

You should contact us at 231.598.8828 if experience worsening redness, significant swelling, blistering, signs of infection, persistent irritation, worsening breakouts, delayed healing, or other concerning symptoms following treatment.

Seek immediate medical attention or call 911 if you experience difficulty breathing, facial swelling, severe allergic reaction, chest pain, or any symptoms you believe may represent a medical emergency.

Eyelash and eyebrow treatments are non-invasive aesthetic services intended to enhance the appearance, shape, definition, fullness, color, and overall appearance of the eyellashes and eyebrows. Treatment techniques, products, and treatment steps vary depending on the service selected, facial anatomy, hair characteristics, treatment goals, and provider assessment.

Services may include shaping, tinting, lamination, lifting, conditioning treatments, or other aesthetic enhancement procedures.

Eyelash and eyebrow treatments may be performed alone or incorporated into broader skincare and aesthetic treatment plans alongside facials, chemical peels, dermaplaning, injectables, skincare products, or other medical and aesthetic treatments.

Eyelash and eyebrow treatments involve the application of professional aesthetic products and techniques intended to shape, lift, define, tint, smooth, or enhance the appearance of the eyelashes and eyebrows.

Treatment techniques, processing times, tint selection, shaping methods, and products vary depending on the treatment selected, hair characteristics, treatment goals, and provider assessment.

Maintenance treatments may be recommended depending on hair growth cycle, treatment selected, and individual response.

As with any aesthetic treatment, eyelash and eyebrow services carry potential risks, side effects, complications, and variable outcomes.

Common treatment responses may include: temporary redness, irritation, tightness, sensitivity, watering of the eyes, skin staining, dryness, tenderness, or temporary discomfort within the treatment area.

Additional risks and complications may include: allergic reaction, irritation, burns, infection, overprocessing of hair, breakage, uneven results, dissatisfaction with cosmetic outcome, or the need for additional treatment or correction.

Treatment may not be appropriate if you:

• Have active eye infection, irritation, rash, sunburn, cuts, open wounds, or inflammation within or near the treatment area.
• Have known allergy or hypersensitivity to treatment products, dyes, adhesives, or ingredients.
• Have recently undergone eye surgery or procedures, unless cleared by your medical provider.
• Have severely sensitive skin or eyes that may not tolerate treatment.

Potential benefits of eyelash and eyebrow treatments may include: enhanced definition, improved shape, fuller appearance, darker appearance, smoother hair appearance, improved symmetry, reduced styling time, and overall aesthetic enhancement of the eye and eyebrow area.

Results vary between individuals and are influenced by natural hair characteristics, treatment consistency, skincare products, lifestyle factors, hair growth cycle, and individual response to treatment. No specific cosmetic result or degree of improvement can be guaranteed.

This treatment is elective and voluntary. You may choose to decline treatment at any time.

Alternative treatment options may include no treatment, makeup products, eyebrow pencils, eyelash serums, false lashes, cosmetic tattooing, or other medical and aesthetic treatments. Each alternative carries its own risks, benefits, limitations, costs, and expected outcomes.

Please arrive without eye makeup, mascara, strip lashes, lash adhesive, eyebrow makeup, or waterproof cosmetics, when possible.

If you wear contact lenses, your provider may recommend removal prior to treatment depending on the service selected.

Mild redness, tightness, sensitivity, dryness, watering of the eyes, or temporary irritation may occur following treatment depending on the treatment selected and individual response.

Use only products recommended or approved by your provider if irritation or sensitivity occurs following treatment.

Avoid rubbing, excessive moisture, aggressive skincare products, or excessive heat exposure around the treatment area immediately following treatment unless otherwise directed by your provider.

Eyelash and eyebrow treatment results are generally visible immediately or within several days following treatment depending on the service selected.

Treatment longevity varies depending on hair growth cycle, skincare products, lifestyle factors, treatment type, and individual response. Maintenance treatments are commonly recommended to help maintain desired results.

Results vary between individuals, and no specific cosmetic result, degree of correction, symmetry, or longevity of results can be guaranteed.

You should contact us at 231.598.8828 if you experience worsening redness, swelling, irritation, eye pain, discharge, blistering, signs of infection, prolonged discomfort, or other concerning symptoms following treatment.

Seek immediate medical attention or call 911 if you experience difficulty breathing, facial swelling, severe allergic reaction, vision changes, severe eye pain, chest pain, or any symptoms you believe may represent a medical emergency.