Label: ELF BEIGE ACNE FIGHTING FOUNDATION- salicylic acid cream
- NDC Code(s): 76354-603-01
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 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, Cyclopentasiloxane, Hydrogenated Polyisobutene, Ethoxydiglycol, Dimethicone, Cyclohexasiloxane, Dimethicone Crossploymer, PEG-10 Dimethicone, Dimethicone PEG 10/15 Crosspolymer, Magnesium Sulfate, Talc, Nylon-12, Phenoxyethanol, Propylene Glycol, Quaternium-18 Benonite, Triethoxycaprylysilane, Methylparaben, Ethylparaben, butylparaben, Propylparaben, Isobutylparaben, Cinnamomum Camphora (Camphor) Bark oil, Melaleuca Alternafolia (Tea Tree) Leaf Oil, Aloe Barbadensis Leaf Jiuce, Hexapeptide-9, Hamamelis Birginiana (Witch Hazel) May Contain: Iron Oxide (CI77491, CI77492, CI77499), Titanium Dioxide
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ELF BEIGE ACNE FIGHTING FOUNDATION
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-603 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) CAMPHOR OIL (UNII: 75IZZ8Y727) DIMETHICONE PEG-10 PHOSPHATE (UNII: O7Q5NJ7X88) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) NYLON-12 (UNII: 446U8J075B) TALC (UNII: 7SEV7J4R1U) PHENOXYETHANOL (UNII: HIE492ZZ3T) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) METHYLPARABEN (UNII: A2I8C7HI9T) ETHYLPARABEN (UNII: 14255EXE39) PROPYLPARABEN (UNII: Z8IX2SC1OH) BUTYLPARABEN (UNII: 3QPI1U3FV8) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) TEA TREE OIL (UNII: VIF565UC2G) ALOE VERA LEAF (UNII: ZY81Z83H0X) WITCH HAZEL (UNII: 101I4J0U34) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-603-01 36 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 12/12/2024 Labeler - e.l.f. Cosmetics, Inc (093902816) Establishment Name Address ID/FEI Business Operations Zhejiang Ayan Biotech Co., Ltd. 544377996 manufacture(76354-603)