Label: SIGNATURE CARE ACNE TREATMENT- salicylic acid liquid
- NDC Code(s): 21130-722-48, 21130-722-77
- Packager: SAFEWAY, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 14, 2023
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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, cocamidopropyl betaine, chamomilla recutita (matricaria) flower extract, cocamidopropyl PG-dimonium chloride phosphate, propylene glycol, aloe barbadensis leaf juice, anthemis nobilis flower extract, C12-15 alkyl lactate, PEG-80 sorbitan laurate, disodium EDTA, benzalkonium chloride, fragrance, yellow 5, red 40.
- Label
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INGREDIENTS AND APPEARANCE
SIGNATURE CARE ACNE TREATMENT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-722 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 ALCOHOL (UNII: 3K9958V90M) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) PEG-80 SORBITAN LAURATE (UNII: 239B50Y732) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMOMILE (UNII: FGL3685T2X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 40 (UNII: WZB9127XOA) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-722-77 177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/26/2012 2 NDC:21130-722-48 258 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/10/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/26/2012 Labeler - SAFEWAY, INC. (009137209)