Replenix Acne
Replenix Acne is an FDA drug label for the active ingredient BENZOYL PEROXIDE manufactured by Topiderm, Inc administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20191031.
Generic: BENZOYL PEROXIDE
Manufacturer: Topiderm, Inc
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 51326-411
Application: M006
Effective: 20191031
Active Ingredients: Active ingredient Benzoyl Peroxide, USP 5%
Indications & Usage
Uses Topical acne medication.
Dosage & Administration
Directions Cleanse the skin thoroughly before applying. Apply a thin layer daily, then gradually increase to two or three times daily. If bothersome drying or peeling occurs, reduce applications. If going outside, use a sunscreen. If irritation or sensitivity develops, discontinue use of both products and consult a doctor.
Contraindications
Not available.
Warnings
Warnings When using this product avoid unnecessary sun exposure and use a sunscreen. For external use only. Keep away from eyes, lips, and mouth. If irritation develops, discontinue use and consult a doctor. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, consult a doctor. May bleach fabrics. Keep out of reach of children. If swallowed, seek professional assistance or contact a Poison Control Center immediately.
Adverse Reactions
Not available.
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