Label: ACNE SCRUB- salicylic acid gel
- NDC Code(s): 55910-821-99
- Packager: Old East Main
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 15, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- use
- Warnings
- When using this product
- Keep out of reach of children
- Directions
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Inactive ingredients
water, sodium C14-16 olefin sulfonate, glycerin, cocamidopropyl betaine, acrylates copolymer, sodium chloride, cellulose, carrageenan, disodium EDTA, Citrus grandis (grapefruit) fruit extract, ascorbyl palmitate, neopentyl glycol dicaprylate/dicaprate, polysorbate 20, polyvinyl alcohol, benzalkonium chloride, butylene glycol, sodium benzotriazolyl butylphenol sulfonate, agar, mica, titanium dioxide, sodium hydroxide, fragrance, red 30, red 40, ext. violet 2
- Adverse reactions
- Disclaimer
- Principal display panel
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INGREDIENTS AND APPEARANCE
ACNE SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-821 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 21 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) SODIUM CHLORIDE (UNII: 451W47IQ8X) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) .ALPHA.-CELLULOSE (UNII: I355QGZ19A) CARRAGEENAN (UNII: 5C69YCD2YJ) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) GRAPEFRUIT (UNII: O82C39RR8C) ASCORBYL PALMITATE (UNII: QN83US2B0N) NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K) POLYSORBATE 20 (UNII: 7T1F30V5YH) POLYVINYL ALCOHOL (100000 MW) (UNII: 949E52Z6MY) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) AGAR (UNII: 89T13OHQ2B) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM HYDROXIDE (UNII: 55X04QC32I) D&C RED NO. 30 (UNII: 2S42T2808B) FD&C RED NO. 40 (UNII: WZB9127XOA) EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-821-99 124 mL in 1 TUBE; Type 0: Not a Combination Product 01/15/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 01/15/2015 Labeler - Old East Main (068331990) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(55910-821)