Label: SIGNATURE CARE OIL FREE ACNE WASH PINK GRAPEFRUIT FOAMING SCRUB- salicylic acid lotion
- NDC Code(s): 21130-734-15
- Packager: Safeway, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 14, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
• cover the entire affected area with a thin layer and rinse thoroughly 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 every other day
- Other Information
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Inactive ingredients
Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Helianthus Annuus (Sunflower) Seed Wax, Acrylates Copolymer, Chondrus Crispus Powder (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, Sodium Chloride, Benzalkonium Chloride, Butylene Glycol, Sodium Benzotriazolyl Butylphenol Sulfonate, Agar, Fragrance, Sodium Hydroxide, Potassium Chloride, Mica, Titanium Dioxide, Red 30, Red 40, Ext. Violet 2
- Label
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INGREDIENTS AND APPEARANCE
SIGNATURE CARE OIL FREE ACNE WASH PINK GRAPEFRUIT FOAMING SCRUB
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-734 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 METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C) HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) PUMMELO (UNII: ET1TN5W71X) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) SODIUM HYDROXIDE (UNII: 55X04QC32I) D&C VIOLET NO. 2 (UNII: 350KA7O6HK) EDETATE DISODIUM (UNII: 7FLD91C86K) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG) FD&C RED NO. 40 (UNII: WZB9127XOA) NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) ASCORBYL PALMITATE (UNII: QN83US2B0N) D&C RED NO. 30 (UNII: 2S42T2808B) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CHONDRUS CRISPUS (UNII: OQS23HUA1X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) POLYSORBATE 20 (UNII: 7T1F30V5YH) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) AGAR (UNII: 89T13OHQ2B) MICA (UNII: V8A1AW0880) POTASSIUM CHLORIDE (UNII: 660YQ98I10) GREEN TEA LEAF (UNII: W2ZU1RY8B0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-734-15 198 mL in 1 TUBE; Type 0: Not a Combination Product 08/13/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/13/2014 Labeler - Safeway, Inc. (009137209)