Label: CLEARSKIN BLEMISH CLEARING FOAMING CLEANSER- salicylic acid gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 10096-0200-1 - Packager: New Avon LLC
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 1, 2019
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
-
WARNINGS
Warnings
For external use onlyWhen using this product
- avoid contact with eyes. If product contacts eyes, rinse thoroughly with water. If irritation persists, seek medical attention
- using other topical acne products at the same time or immediately after this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor
-
DOSAGE & ADMINISTRATION
Directions
- wet hands and face with warm water
- squeeze an appropriate amount of product onto wet hands
- lather onto skin with a gentle, circular motion, and leave on for 30 seconds
- rinse with warm water and gently pat dry. May be used once a day.
- if bothersome dryness, irritation or peeling occurs, reduce application to every other day
-
INACTIVE INGREDIENT
Inactive ingredients
WATER/EAU
SODIUM C14-16 OLEFIN SULFONATE
GLYCERIN
COCAMIDOPROPYL BETAINE
SODIUM METHYL COCOYL TAURATE
ACRYLATES COPOLYMER
SODIUM CHLORIDE
TRITICUM VULGARE (WHEAT) GERM EXTRACT
GLYCOL DISTEARATE
SODIUM LAUROAMPHOACETATE
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE
MENTHYL LACTATE
CITRIC ACID
DISODIUM EDTA
SODIUM HYDROXIDE
SODIUM CITRATE
BENZOIC ACID
PARFUM/FRAGRANCE
RED 33/CI 17200
BLUE 1/CI 42090 - QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CLEARSKIN BLEMISH CLEARING FOAMING CLEANSER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0200-1 125 mL in 1 TUBE; Type 0: Not a Combination Product 01/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/02/2010 Labeler - New Avon LLC (080143520)