OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Salicylic Acid 1%
Active Ingredient
Salicylic Acid 1%
Purpose
Acne treatment cream
Uses: for the management of acne
Warnings: For external use only.
When using this product:
Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
Clean the skin thoroughly before applying this product.
Cover the entire affected area with a thin layer one to three times daily.
Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
Water/Aqua/Eau, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Glycerin, Butyrospermum Parkii, Glycereth-26, Persea Gratissima Oil, Simmondsia Chinensis Seed Oil, Olea Europaea Fruit Oil, Cetearyl Olivate, Sorbitan Olivate, Tetrapeptide-21, Glucosamine HCl, Orchis Morio Flower Extract, Cucumis Sativus Fruit Extract, Zingiber Officinale Root Extract, Salix Alba Bark Extract, Algae Extract, Yeast Extract, Sodium Hyaluronate, Tetrahexyldecyl Ascorbate, Tocopheryl Acetate, Panthenol, Hydrolyzed Ceasalpinia Spinosa Gum, Caesalpinia Spinosa Gum, Arginine, Sorbitan Palmitate, Bisabolol, Synthetic Urea, Ammonium Acryloyldimethyltaurate/VP Copolymer, Dimethicone, Ceteth-10 Phosphate, Dicetyl Phosphate, Cetyl Palmitate, Tetrasodium EDTA, Phenoxyethanol, Ethylhexylgycerin, Hexylene Glycol, Caprylyl Glycol, Fragrance.
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72644-622 | 72644-622-30 |
Every source-derived ingredient row is available through these pages.
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| a945003c-a0fe-49d3-8770-207eebb13c8b | 1175d9d6-3137-47d5-89be-3f2a7c2a7451 | 2018-09-21 | Warnings | a945003c-a0fe-49d3-8770-207eebb13c8b 1175d9d6-3137-47d5-89be-3f2a7c2a7451 |
Adverse event summaries are temporarily unavailable. Other product information remains available.