Label: ACNE CLEARING CLEANSER- salicylic acid gel
- NDC Code(s): 84262-010-01
- Packager: GLYTONE LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 28, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Use
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Warnings
For external use only.
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Directions
- Dispense a small amount into hand and mix with a little water.
- Apply a thin layer over the entire affected area in a circular motion and rinse thoroughly with warm water two times daily.
- Because excessive dry of the skin may occur, start with one application daily, then gradually increase to two 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.
- Other Information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ACNE CLEARING CLEANSER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84262-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 2 mL Inactive Ingredients Ingredient Name Strength LAURIC ACID (UNII: 1160N9NU9U) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) METHYLPROPANEDIOL (UNII: N8F53B3R4R) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPANEDIOL (UNII: 5965N8W85T) CLEOME GYNANDRA LEAF (UNII: 505381240S) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) HEXYLENE GLYCOL (UNII: KEH0A3F75J) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) SODIUM HYDROXIDE (UNII: 55X04QC32I) XYLITYLGLUCOSIDE (UNII: O0IEZ166FB) EDETATE SODIUM (UNII: MP1J8420LU) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84262-010-01 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 03/01/2024 Labeler - GLYTONE LLC (119226548) Registrant - GLYTONE LLC (119226548)