Label: CHARCOAL BLACKHEAD CLEARING SCRUB- salicylic acid cream
- NDC Code(s): 69842-910-28
- Packager: CVS Pharmacy, 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 September 11, 2023
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- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, sodium laureth sulfate, polylactic acid, acrylates copolymer, sodium chloride, coco-betaine, cocamide MEA, glycerin, charcoal powder, citric acid, polyglycerin-10, polyglyceryl-10 myristate, polyglyceryl-10 stearate, PPG-5-ceteth-20, sodium hydroxide, trisodium ethylenediamine disuccinate, microcrystalline cellulose, cellulose, fragrance, iron oxides
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INGREDIENTS AND APPEARANCE
CHARCOAL BLACKHEAD CLEARING SCRUB
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-910 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20.6 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) POLYLACTIDE (UNII: 459TN2L5F5) METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J) SODIUM CHLORIDE (UNII: 451W47IQ8X) COCO-BETAINE (UNII: 03DH2IZ3FY) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCERIN (UNII: PDC6A3C0OX) ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POLYGLYCERIN-10 (UNII: P9060O936A) POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91) PPG-5-CETETH-20 (UNII: 4AAN25P8P4) SODIUM HYDROXIDE (UNII: 55X04QC32I) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POWDERED CELLULOSE (UNII: SMD1X3XO9M) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-910-28 148 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/01/2016 Labeler - CVS Pharmacy, Inc. (062312574) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(69842-910) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(69842-910)