Label: ELF CLEAR BLEMISH CONTROL FACE PRIMER- salicylic acid cream
- NDC Code(s): 76354-624-01
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions:
Cleanse the skin thoroughly before applying medication. Cover the entire affected area with a thin layer one to three times daily. Because excessive drying of 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.
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INACTIVE INGREDIENT
Inactive Ingredient:
Water, Hydrogenated Polyisobutene, Dimethicone, Butylene Glycol, Ethoxydiglycol, Propylene Glycol, Magnesium Aluminum Silicate, Cetearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Tyiethanolamine, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, VP/Hexadecene Coplymer, Tocopheryl Acetate (VE), Stearic Acid, Xanthan Gum, Silica, Disodium EDTA, Panthenol, Rosmarinus Officinalis (Rosemary) Extract, Thymus Vulgaris (Thyme) Extract, Melaleuca Alternafolia (Tea Tree) Extract, Citrus Limon (Lemon) Peel Extract, Phenoxyethanol, Caprylyl Glycol
- Package Labeling: ELF CLEAR BLEMISH CONTROL FACE PRIMER 14ml 76354-624-01
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INGREDIENTS AND APPEARANCE
ELF CLEAR BLEMISH CONTROL FACE PRIMER
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-624 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength HYDROGENATED POLYBUTENE (370 MW) (UNII: V5H8103878) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) PEG-100 STEARATE (UNII: YD01N1999R) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) STEARIC ACID (UNII: 4ELV7Z65AP) XANTHAN GUM (UNII: TTV12P4NEE) DISODIUM HEDTA (UNII: KME849MC7A) PANTHENOL (UNII: WV9CM0O67Z) ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O) THYMUS CITRIODORUS LEAF (UNII: 2J04LZ7UPZ) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-624-01 14 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 10/10/2015 Labeler - e.l.f. Cosmetics, Inc (093902816) Registrant - Zhejiang Ayan Biotech Co.,Ltd. (544377996) Establishment Name Address ID/FEI Business Operations Zhejiang Ayan Biotech Co.,Ltd. 544377996 manufacture(76354-624)