Label: ACNE SCRUB- salicylic acid gel
- NDC Code(s): 50594-821-99
- Packager: Big Lots
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 26, 2024
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- Active ingredient
- Purpose
- use
- Warnings
- When using this product
- Keep out of reach of children
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Inactive ingredients
water, sodium C14-16 olefin sulfonate, glycerin, cocamidopropyl betaine, acrylates copolymer, sodium chloride, microcrystalline cellulose, cellulose, carrageenan, C12-15 alkyl lactate, disodium EDTA, cocamidopropyl PG-dimonium chloride phosphate, Citrus grandis (grapefruit) fruit extract, polyquaternium-7, Camellia sinensis leaf extract, ascorbyl palmitate, neopentyl glycol dicaprylate/dicaprate, Anthemis nobilis flower extract, polysorbate 20, polyvinyl alcohol, propylene glycol, benzalkonium chloride, butylene glycol, sodium benzotriazolyl butylphenol sulfonate, agar, mica, titanium dioxide, sodium hydroxide, fragrance, red 30, red 40, ext. violet 2
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INGREDIENTS AND APPEARANCE
ACNE SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50594-821 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) METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C) SODIUM CHLORIDE (UNII: 451W47IQ8X) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POWDERED CELLULOSE (UNII: SMD1X3XO9M) CARRAGEENAN (UNII: 5C69YCD2YJ) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) EDETATE DISODIUM (UNII: 7FLD91C86K) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) GRAPEFRUIT (UNII: O82C39RR8C) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ASCORBYL PALMITATE (UNII: QN83US2B0N) NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K) CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG) POLYSORBATE 20 (UNII: 7T1F30V5YH) POLYVINYL ALCOHOL (UNII: 532B59J990) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 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:50594-821-99 124 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 - Big Lots (017885351) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(50594-821) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(50594-821)