Label: NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - DEEP 20- salicylic acid liquid
- NDC Code(s): 69968-0338-1
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- Clean the skin thoroughly before applying this product
- 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
- Other Information
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Inactive ingredients
Water, cyclopentasiloxane, dimethicone, kaolin, VP/hexadecene copolymer, synthetic wax, cetyl PEG/PPG-10/1 dimethicone, trisiloxane, BIS-PEG/PPG-14/14 dimethicone, cyclohexasiloxane, butylene glycol, silica, phenoxyethanol, boron nitride, polysilicone-11, quaternium-90 bentonite, sodium chloride, magnesium sulfate, methylparaben, farnesol, chamomilla recutita (matricaria) flower extract, propylene carbonate, triethoxycaprylylsilane, propylparaben, aloe barbadensis leaf juice, polymethyl methacrylate, tocopheryl acetate, cocamidopropyl PG-dimonium chloride phosphate, cetyl lactate, C12-15 alkyl lactate, benzalkonium chloride, retinyl palmitate, pantothenic acid, ascorbic acid,titanium dioxide, iron oxides
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1.4 g Vial Blister Pack
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INGREDIENTS AND APPEARANCE
NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - DEEP 20
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0338 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE (UNII: 92RU3N3Y1O) KAOLIN (UNII: 24H4NWX5CO) VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9) TRISILOXANE (UNII: 9G1ZW13R0G) BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE) CYCLOMETHICONE 6 (UNII: XHK3U310BA) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PHENOXYETHANOL (UNII: HIE492ZZ3T) BORON NITRIDE (UNII: 2U4T60A6YD) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) SODIUM CHLORIDE (UNII: 451W47IQ8X) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) METHYLPARABEN (UNII: A2I8C7HI9T) FARNESOL (UNII: EB41QIU6JL) CHAMOMILE (UNII: FGL3685T2X) PROPYLENE CARBONATE (UNII: 8D08K3S51E) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) PROPYLPARABEN (UNII: Z8IX2SC1OH) ALOE VERA LEAF (UNII: ZY81Z83H0X) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) CETYL LACTATE (UNII: A7EVH2RK4O) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) PANTOTHENIC ACID (UNII: 19F5HK2737) ASCORBIC ACID (UNII: PQ6CK8PD0R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) QUATERNIUM-90 BENTONITE (UNII: 97K5YEF88C) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0338-1 1.4 in 1 BLISTER PACK 10/02/2017 1 1.4 g in 1 VIAL; 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 10/02/2017 Labeler - Kenvue Brands LLC (118772437)
