Buy Cutivate
Cutivate

35
A potent steroid cream used to treat various inflammatory skin conditions like eczema.


Ingredient
Category
Availability
In Stock
Delivery
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Alternative/Local Brand
Cutivate
Active Ingredient(s)
Fluticasone
Primary Category
Skin Treatment
Therapeutic Class
Corticosteroids, potent (group III)
Pharmacological Class
Topical corticosteroids
Indications
Eczema, Psoriasis, Dermatitis, Skin rashes
Contraindications
Untreated skin infections, Rosacea, Acne vulgaris, Skin itching without inflammation
Minor Side Effects
Stinging, Burning, Dryness
Moderate Side Effects
Skin thinning, Stretch marks, Changes in skin colour, Excessive hair growth
Serious Side Effects
Severe allergic reaction, Skin infection spread, Adrenal suppression (long-term use), Blurred vision
Dosage Forms
Cream, Ointment
Administration Route
Topical
Mechanism of Action
It reduces inflammation, redness, and itching by inhibiting the release of chemicals that cause the immune response in the skin.
Prescription Status
Rx
Manufacturer
GlaxoSmithKline
Patient Summary
A potent steroid cream used to treat various inflammatory skin conditions like eczema.
Onset Time
1-2 days
Duration
Up to 12 hours
Storage Instructions
Store below 30°C; do not freeze.
Drug Interactions
Ritonavir, Itraconazole
Age Restrictions
Suitable for infants over 3 months, children, and adults
Pregnancy Use
Use sparingly and for short periods.
Alternative Drugs
Betamethasone, Hydrocortisone, Mometasone

What is Cutivate?

Cutivate is a topical skin-care medication that contains fluticasone as its active ingredient. Fluticasone belongs to the class of synthetic corticosteroids and is formulated as a cream in a tube with 10 g or 20 g strengths. In Hong Kong, Cutivate is a prescription-only product (Rx) and is regulated by the Department of Health under the Pharmaceutical Service. It is used to treat inflammatory skin conditions by reducing redness, swelling, and itching.

How Cutivate Works in the Body

Fluticasone is a potent glucocorticoid that binds to intracellular glucocorticoid receptors in the skin. This binding:

  • Modulates gene transcription, leading to decreased production of inflammatory cytokines and prostaglandins.
  • Suppresses the migration of immune cells (e.g., neutrophils, eosinophils) to the site of irritation.
  • Reduces capillary dilation, which lessens erythema (redness).

Because the drug is applied locally, systemic absorption is minimal, allowing targeted anti-inflammatory effects with a lower risk of systemic side effects compared with oral steroids. The onset of action is typically within a few hours, with maximal effect after several days of consistent use.

Conditions Treated by Cutivate

Cutivate is approved in Hong Kong for the topical management of the following dermatologic indications:

  • Atopic dermatitis (eczema)
  • Psoriasis plaques (particularly mild-to-moderate)
  • Seborrheic dermatitis
  • Contact dermatitis
  • Stasis dermatitis

These indications are based on the drug’s anti-inflammatory and immunosuppressive properties, which help control the chronic inflammation that characterises these skin conditions.

Off-Label and Investigational Applications

Evidence from peer-reviewed dermatology literature suggests that topical fluticasone may be effective for:

  • Lichen planus (off-label) - limited case series support use under specialist supervision.
  • Discoid lupus erythematosus (off-label) - small trials indicate reduction of lesions when combined with standard therapy.

These uses are not approved by the Hong Kong Department of Health. Off-label use requires medical supervision and individualized risk assessment.

Who Should (Not) Use Cutivate?

Ideal Candidates

  • Adults and adolescents with the approved inflammatory skin conditions listed above.
  • Patients whose lesions are confined to areas amenable to topical therapy.

Absolute Contraindications

  • Known hypersensitivity to fluticasone or any excipients in the formulation.
  • Viral skin infections (e.g., herpes simplex, varicella-zoster) in the treatment area.
  • Untreated fungal or bacterial skin infections.

Relative Contraindications

  • Pregnant or breastfeeding individuals - corticosteroids cross the placenta and may be secreted in breast milk; risk-benefit assessment is needed.
  • Children under 12 years - higher risk of systemic absorption and growth suppression; use only when clearly indicated.
  • Areas of thin skin (e.g., eyelids, genitalia) - increased risk of skin atrophy.

Special Populations

  • Elderly: May require reduced frequency due to thinner dermis.
  • Patients with hepatic or renal impairment: No dose adjustment is needed for topical use, but monitor for systemic effects if large body surface areas are treated.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Transient burning, stinging, or itching at the application site.
  • Dryness or peeling of the skin.

Serious Adverse Events

  • Skin atrophy (thinning), striae (stretch marks), telangiectasia (visible blood vessels).
  • Secondary infection (bacterial, fungal, or viral) due to local immunosuppression.
  • Hypothalamic-pituitary-adrenal (HPA) axis suppression when large surface areas are treated for prolonged periods.

Drug Interactions

  • Major: Concurrent use of other potent topical corticosteroids may increase systemic exposure.
  • Moderate: topical calcineurin inhibitors (e.g., tacrolimus) can have additive immunosuppressive effects; monitor for infection.
  • Mechanism: Overlapping metabolism pathways are not a concern for topical fluticasone, but systemic absorption could be altered by extensive use of CYP3A4-inducing agents (e.g., rifampin) in rare cases.

Food and Lifestyle Interactions

  • No known dietary restrictions.
  • Alcohol consumption does not affect topical absorption but may exacerbate skin irritation in some individuals.
  • Patients should avoid applying Cutivate to damaged skin that is exposed to sunlight for prolonged periods, as corticosteroids can increase photosensitivity.

If you are taking other medications, especially systemic steroids or immunosuppressants, inform your healthcare provider before starting Cutivate.

How to Take Cutivate

  • Standard dosing: Apply a thin layer of the cream to the affected area once or twice daily, as directed by your clinician.
  • Amount guidance: A fingertip unit (approximately 0.5 g) typically covers an area the size of an adult palm.
  • Special populations:
  • Elderly or children: Use the lowest effective frequency (often once daily).
  • Extensive body-surface involvement: Limit use to ≤ 2 weeks without medical review; longer courses may require intermittent dosing or a step-down to a lower-potency steroid.
  • Administration tips:
  • Wash hands before and after application.
  • Do not cover the treated area with occlusive dressings unless instructed, as this can increase absorption.
  • Missed dose: Apply as soon as remembered if within 12 hours; otherwise, skip and resume the regular schedule. Do not double the dose.
  • Overdose: Signs include widespread skin thinning, severe bruising, or systemic Cushingoid features. Seek urgent medical care; treatment is supportive and may involve tapering systemic steroids if necessary.
  • Discontinuation: For prolonged therapy, taper the frequency (e.g., every other day) to avoid rebound inflammation.

Monitoring and Follow-Up

  • Short-term use (≤ 2 weeks): Usually no laboratory monitoring required.
  • Long-term or extensive use: Periodic assessment of skin integrity (checking for atrophy, striae) and, if systemic absorption is suspected, morning serum cortisol may be measured.
  • When to seek help: New signs of infection, worsening skin appearance, or systemic symptoms such as unexplained weight gain or mood changes.

Storage and Handling

  • Keep the tube at room temperature (15-30 °C) away from direct sunlight and excess moisture.
  • Seal the cap tightly after each use to prevent contamination.
  • Store out of reach of children and pets.
  • Do not use the product past the expiry date printed on the packaging.
  • For disposal, follow local pharmacy take-back programs or the Hong Kong Waste Disposal Ordinance guidelines.

Medication-Specific Glossary

Potency
A classification of corticosteroids based on their anti-inflammatory strength; fluticasone is considered a high-potency topical steroid.
Atrophogenic
Refers to the capacity of a drug to cause thinning of the skin with prolonged use.
Corticosteroid-Induced HPA Suppression
Reduced activity of the body’s own cortisol production due to systemic absorption of topical steroids.
Occlusion
The covering of a treated skin area with a dressing that traps moisture and heat, potentially increasing drug absorption.

Medical Disclaimer

This article provides educational information about Cutivate and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Cutivate FAQ

Can Cutivate be used on the face?

Cutivate is a high-potency steroid, so routine facial use is generally discouraged due to the risk of skin atrophy and telangiectasia. If facial application is deemed necessary, a dermatologist will prescribe the shortest possible duration and closely monitor for side effects.

Does using Cutimize affect drug testing for athletes?

Topical fluticasone can be detected in urine only after extensive application over large body areas. For most athletes, occasional therapeutic use is unlikely to trigger a positive result, but it is advisable to disclose all medications to the relevant sports authority.

What inactive ingredients are in the Cutivate tube?

The formulation typically contains emulsifiers, preservatives (e.g., phenoxyethanol), and moisturising agents such as glycerin. Exact excipient lists are provided in the product’s package insert.

Is it safe to apply Cutivate after swimming or showering?

Yes, but the skin should be gently patted dry before application. Applying to wet skin may dilute the dose and reduce efficacy.

Can Cutivate be used during pregnancy?

Topical corticosteroids can cross the placenta, especially when used over large areas or for prolonged periods. Pregnant patients should only use Cutivate if the potential benefit outweighs the potential risk, under obstetric guidance.

How does Cutivate differ from other topical steroids like betamethasone?

Fluticasone has a higher receptor affinity and longer skin-residence time, giving it a higher potency classification than many mid-potency steroids such as betamethasone dipropionate.

Store at room temperature (15-30 °C). Do not refrigerate or expose the tube to extreme heat, as this can alter the cream’s consistency.

Are there any known drug interactions if I’m also using a topical antifungal?

Concurrent use may increase the risk of local infection because corticosteroids suppress immune responses. If an antifungal is required, alternate the applications (e.g., morning antifungal, evening steroid) or use a combined preparation if approved.

Can I travel internationally with Cutivate?

Yes, but keep the tube in its original packaging with the prescription label visible. Some countries may require a copy of the prescribing physician’s note for controlled skin-care products.

Why does Cutivate come in 10 g and 20 g tubes?

The different sizes allow clinicians to match the prescribed amount to the extent and severity of the disease, helping to limit waste and reduce the risk of over-use.

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