Label: BLEMISH CONTROL BASICS KIT- salicylic acid kit
- NDC Code(s): 76354-415-02, 76354-416-02, 76354-417-01
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 24, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
- Warnings
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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 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. Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated eleswhere on this label.
- Inactive ingredients
- Questions or comments
- Drug Facts
- Active ingredients
- Uses
- Warnings
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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 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. Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated eleswhere on this label.
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Inactive ingredients
Water (Aqua), Niacinamide, Glycerin, Silica, Propanediol, Isododecane, Tranexamic Acid, Glyceryl Stearate Citrate, C12-15 Alkyl Benzoate, Acetyl Glucosamine, Tromethamine, Aluminum Starch Octenylsuccinate, Phenoxyethanol, Cetearyl Alcohol, Capryloyl Glycine, Potassium Cetyl Phosphate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Xanthan Gum, Caprylyl Glycol, Ethylhexylglycerin, Tocopherol, Helianthus Annuus (Sunflowe) Seed Oil, Disodium EDTA, Caprylic Acid, Sodium Citrate May Contain: Chromium Oxide Greens (CI 77288), Iron Oxides (CI 77492)
- Questions or comments
- Package Labeling: Kit
- Package Labeling: 30ml
- Package Labeling: 30ml
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INGREDIENTS AND APPEARANCE
BLEMISH CONTROL BASICS KIT
salicylic acid kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-417 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-417-01 1 in 1 KIT 02/25/2022 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 1 BOTTLE 30 mL Part 1 of 2 ACNE CLARIFYING CLEANSER
salicylic acid liquidProduct Information Item Code (Source) NDC:76354-415 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) ZINC PIDOLATE (UNII: C32PQ86DH4) SODIUM BENZOATE (UNII: OJ245FE5EU) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM CHLORIDE (UNII: 451W47IQ8X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) NIACINAMIDE (UNII: 25X51I8RD4) TRANEXAMIC ACID (UNII: 6T84R30KC1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-415-02 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 02/25/2022 Part 2 of 2 ACNE CALMING WATER CREAM
salicylic acid creamProduct Information Item Code (Source) NDC:76354-416 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) NIACINAMIDE (UNII: 25X51I8RD4) GLYCERIN (UNII: PDC6A3C0OX) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PROPANEDIOL (UNII: 5965N8W85T) ISODODECANE (UNII: A8289P68Y2) TRANEXAMIC ACID (UNII: 6T84R30KC1) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) N-ACETYLGLUCOSAMINE (UNII: V956696549) TROMETHAMINE (UNII: 023C2WHX2V) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) ALLANTOIN (UNII: 344S277G0Z) XANTHAN GUM (UNII: TTV12P4NEE) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) TOCOPHEROL (UNII: R0ZB2556P8) SUNFLOWER OIL (UNII: 3W1JG795YI) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CAPRYLIC ACID (UNII: OBL58JN025) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-416-02 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 02/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 02/25/2022 Labeler - e.l.f. Cosmetics, Inc (093902816)
