

Retin A 0,05
| Product dosage: 20g | |||
|---|---|---|---|
| Package (num) | Per tube | Price | Buy |
| 3 | $23.33 | $70.00 (0%) | 🛒 Add to cart |
| 10 | $15.00 | $233.33 $150.00 (36%) | 🛒 Add to cart |
| 15 | $13.80 | $350.00 $207.00 (41%) | 🛒 Add to cart |
| 20 | $13.20
Best per tube | $466.67 $264.00 (43%) | 🛒 Add to cart |
Synonyms | |||
Retin A 0.05: Advanced Topical Retinoid for Acne and Photoaging
Retin A 0.05% cream contains tretinoin, a first-generation retinoid and the gold-standard topical treatment for both inflammatory acne and photoaging. As a prescription-only medication, it works by normalizing keratinization, reducing microcomedone formation, and stimulating collagen production through binding to retinoic acid receptors in the skin. This formulation is specifically indicated for patients requiring a moderate strength option, balancing efficacy with tolerability for sustained dermatological therapy.
Features
- Active ingredient: Tretinoin 0.05% w/w
- Pharmaceutical form: Topical cream
- Vehicle: Oil-in-water emulsion base
- Prescription status: Rx-only
- Packaging: 20g and 45g aluminum tubes
- Stability: Photolabile; requires opaque packaging
Benefits
- Significantly reduces inflammatory and non-inflammatory acne lesions by unblocking follicles and preventing comedone formation
- Improves skin texture and tone through epidermal remodeling and increased collagen synthesis
- Diminishes visible signs of photoaging including fine lines, wrinkles, and actinic keratoses
- Evens skin pigmentation by dispersing melanin granules and reducing melanocyte activity
- Prevents new acne formation through sustained follicular epithelium normalization
- Enhances penetration of other topical agents through stratum corneum modulation
Common use
Retin A 0.05% is primarily prescribed for the treatment of acne vulgaris grades I-III, characterized by comedones, papules, and pustules. It is equally indicated for the mitigation of cutaneous damage caused by chronic sun exposure, including fine wrinkling, mottled hyperpigmentation, and tactile roughness of facial skin. Off-label uses include management of keratosis pilaris, pityriasis rubra pilaris, and certain forms of ichthyosis. The 0.05% concentration represents an intermediate potency option, typically prescribed after evaluating patient tolerance to lower strengths or for patients with moderate photodamage.
Dosage and direction
Apply a pea-sized amount once daily, preferably in the evening, to thoroughly cleansed and dried facial skin. Dot the medication evenly across forehead, cheeks, chin, and nose, then spread gently to cover entire treatment area. Avoid application to eyelids, lips, and mucous membranes. Initiate therapy with application every second or third night for the first 2-3 weeks to assess tolerance before progressing to nightly use. Patients should allow the cream to absorb fully for 20-30 minutes before applying other topical products. Duration of treatment continues indefinitely for anti-aging benefits, while acne treatment typically spans 8-12 weeks for initial response with maintenance therapy as needed.
Precautions
Discontinue use if hypersensitivity reactions occur including severe erythema, edema, or blistering. Patients should minimize sunlight exposure during treatment and use broad-spectrum sunscreen (SPF 30+) daily due to increased photosensitivity. Avoid concomitant use of other potentially irritating topical products (including abrasives, astringents, and high-concentration alpha hydroxy acids) unless directed by a dermatologist. Not recommended for use on eczematous, sunburned, or broken skin. Caution should be exercised when treating patients with personal or family history of skin cancer. Pregnancy should be excluded before initiation due to potential systemic absorption and teratogenic risk.
Contraindications
Absolute contraindications include hypersensitivity to tretinoin or any component of the formulation. Relative contraindications include pregnancy (Category C), breastfeeding, and patients with history of eczema, rosacea, or other chronic dermatoses that may compromise skin barrier function. Not recommended for patients with sun-sensitive conditions such as lupus erythematosus or porphyria. Should not be used concomitantly with photosensitizing medications including thiazides, tetracyclines, fluoroquinolones, and phenothiazines.
Possible side effects
Expected initial reactions include erythema, peeling, dryness, and burning/stinging sensation (retinization period), typically peaking at 2-4 weeks and subsiding by 8 weeks. Persistent side effects may include photosensitivity, skin irritation, and paradoxical acne flare during initial weeks. Less common effects include temporary hyperpigmentation or hypopigmentation, blistering, and crusting. Rare systemic effects include headache and photosensitivity reactions. Most cutaneous side effects are dose-dependent and manageable with application frequency adjustment and moisturization.
Drug interaction
Concurrent use with benzoyl peroxide may oxidize tretinoin, reducing efficacy—apply at different times of day. Enhanced absorption and potential irritation may occur with concomitant topical corticosteroids, sulfur, resorcinol, or salicylic acid. Systemic interactions are unlikely due to minimal absorption, though caution is advised with vitamin A supplements due to potential additive effects. Increased photosensitivity may occur with other phototoxic agents including tetracyclines, fluoroquinolones, and sulfonamides.
Missed dose
Apply as soon as remembered if same evening. If next application time is near, skip missed dose and resume regular schedule. Do not double application to compensate for missed dose. Consistent application is important for therapeutic effect, but occasional missed doses will not significantly impact long-term outcomes. Patients should maintain regular application schedule once skin has acclimated to treatment.
Overdose
Topical overdose may cause severe erythema, peeling, discomfort, and edema. Management involves immediate discontinuation, gentle cleansing, and application of bland emollients until symptoms resolve. Oral ingestion, though unlikely, may cause symptoms similar to hypervitaminosis A including headache, nausea, vomiting, and dizziness. In case of accidental ingestion, seek medical attention immediately for supportive care. There is no specific antidote for tretinoin overdose.
Storage
Store at controlled room temperature (15-30°C) in original tube with cap tightly closed. Protect from light and freezing. Keep away from heat sources and sunlight. Do not store in bathroom where humidity and temperature fluctuations may degrade the product. Keep out of reach of children and pets. Discard any medication that has changed color or consistency. Do not use after expiration date printed on packaging.
Disclaimer
This information describes tretinoin 0.05% cream for educational purposes only and does not replace professional medical advice. Consultation with a qualified healthcare provider is essential before starting any prescription medication. Individual results may vary based on skin type, condition severity, and adherence to treatment protocol. Proper diagnosis and monitoring by a dermatologist are required for safe and effective use. Not all side effects or interactions are listed here—report any unexpected reactions to your healthcare provider immediately.
Reviews
Clinical studies demonstrate 60-80% reduction in acne lesions after 12 weeks of treatment with tretinoin 0.05% cream. In photoaging studies, 74% of patients showed significant improvement in fine wrinkles after 24 weeks. Dermatologist ratings consistently show good to excellent efficacy in 85% of patients with moderate acne. Patient-reported satisfaction scores indicate high satisfaction with texture improvement (78%) and acne reduction (82%), though initial irritation leads to 15% discontinuation rate. Long-term studies confirm maintained efficacy with continuous use for up to 48 weeks without tolerance development.





