Label: ALMAY CLEAR COMPLEXION BLEMISH ARMOR- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 0311-0722-13 - Packager: Almay, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 August 1, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredients
- Warnings
- When using this product:
- Keep out of reach of children
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Directions
- Cleanse skin throughly before applying the product
- Cover the entire affected area with a this 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 even every other day
- For new users: apply product sparingly to one or two small affected areas during first 3 days. If no discomfort occurs, follow directions above
- Cleanse skin throughly before applying the product
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Inactive Ingredients
Aqua/Water/Eau, Polysilicone-11, Polymethylsilsesquioxane/Silica Crosspolymer, Alcohol Denat, Styrene/Acrylates Copolymer, Hydrolyzed Vegetable Protein, Phenoxyethanol, Caprylyl Glycol, Xantam gum, Laureth-12, Lecithin, Tocopheryl Acetate, Sorbic Acid, Sclerotium Gum, Trisodium EDTA, Butylene Glycol, Pullulan, Citric Acid, Sodium Dehydroacetate, Ethylhexylglycerin, Silica, Lysolecithin, Hydrogenated Phosphatidylcholine, Enantia Chlorantha Bark Extract, Saccharide Isomerate
- Use
- DOSAGE & ADMINISTRATION
- Purpose
- Packaging
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INGREDIENTS AND APPEARANCE
ALMAY CLEAR COMPLEXION BLEMISH ARMOR
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0311-0722 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 mg in 2 mL Inactive Ingredients Ingredient Name Strength STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) AMMONIUM LAURETH-12 SULFATE (UNII: E1ZP93931S) POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK) POLYSILICONE-15 (UNII: F8DRP5BB29) WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALUMINUM SILICATE (UNII: T1FAD4SS2M) SORBIC ACID (UNII: X045WJ989B) EDETATE TRISODIUM (UNII: 420IP921MB) CAPRYLYL GLYCOL (UNII: 00YIU5438U) XANTHAN GUM (UNII: TTV12P4NEE) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PULLULAN (UNII: 8ZQ0AYU1TT) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) SACCHARIDE ISOMERATE (UNII: W8K377W98I) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CITRIC ACID ACETATE (UNII: DSO12WL7AU) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0311-0722-13 38 mL in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product 06/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 06/01/2018 Labeler - Almay, Inc. (064988652) Establishment Name Address ID/FEI Business Operations REVLON, INC. 809725570 manufacture(0311-0722)