Label: NEUTROGENA SKINCLEARING MINERAL POWDER - HONEY 85- salicylic acid cream
NEUTROGENA SKINCLEARING MINERAL POWDER - CHESTNUT 135- salicylic acid cream
- NDC Code(s): 69968-0339-1, 69968-0340-1
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 13, 2023
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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
Dimethicone, Zinc Stearate, Polyethylene, Octyldodecyl Stearoyl Stearate, C12-15 Alkyl Benzoate, Polysilicone-11, Nylon-12, Petrolatum, Ethylene/Acrylic Acid Copolymer, Calcium Silicate, Methylparaben, Sodium Dehydroacetate, Tocopheryl Acetate, Retinyl Palmitate, Propylparaben, Panthenol, Polymethyl Methacrylate, Ascorbyl Palmitate, C12-15 Alkyl Lactate, Cetyl Lactate, Benzalkonium Chloride, Cocamidopropyl PG-Dimonium Chloride Phosphate, Ascorbic Acid, Pantothenic Acid, Talc, Iron Oxides, Mica, Zinc Oxide.
May Contain: Titanium Dioxide, Carmine.
- Questions ?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 11 g Container Label - Honey 85
- PRINCIPAL DISPLAY PANEL - 11 g Container Label - Chestnut 135
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INGREDIENTS AND APPEARANCE
NEUTROGENA SKINCLEARING MINERAL POWDER - HONEY 85
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0339 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 TALC (UNII: 7SEV7J4R1U) DIMETHICONE (UNII: 92RU3N3Y1O) ZINC STEARATE (UNII: H92E6QA4FV) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C) MICA (UNII: V8A1AW0880) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) NYLON-12 (UNII: 446U8J075B) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) PETROLATUM (UNII: 4T6H12BN9U) ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I) CALCIUM SILICATE (UNII: S4255P4G5M) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) METHYLPARABEN (UNII: A2I8C7HI9T) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PROPYLPARABEN (UNII: Z8IX2SC1OH) PANTHENOL (UNII: WV9CM0O67Z) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) CETYL LACTATE (UNII: A7EVH2RK4O) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) ASCORBYL PALMITATE (UNII: QN83US2B0N) PANTOTHENIC ACID (UNII: 19F5HK2737) ASCORBIC ACID (UNII: PQ6CK8PD0R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) ZINC OXIDE (UNII: SOI2LOH54Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0339-1 11 g in 1 CONTAINER; Type 0: Not a Combination Product 10/02/2017 01/31/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 10/02/2017 01/31/2021 NEUTROGENA SKINCLEARING MINERAL POWDER - CHESTNUT 135
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0340 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 TALC (UNII: 7SEV7J4R1U) DIMETHICONE (UNII: 92RU3N3Y1O) ZINC STEARATE (UNII: H92E6QA4FV) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C) MICA (UNII: V8A1AW0880) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) NYLON-12 (UNII: 446U8J075B) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) PETROLATUM (UNII: 4T6H12BN9U) ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I) CALCIUM SILICATE (UNII: S4255P4G5M) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) METHYLPARABEN (UNII: A2I8C7HI9T) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PROPYLPARABEN (UNII: Z8IX2SC1OH) PANTHENOL (UNII: WV9CM0O67Z) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) CETYL LACTATE (UNII: A7EVH2RK4O) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) ASCORBYL PALMITATE (UNII: QN83US2B0N) PANTOTHENIC ACID (UNII: 19F5HK2737) ASCORBIC ACID (UNII: PQ6CK8PD0R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) ZINC OXIDE (UNII: SOI2LOH54Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0340-1 11 g in 1 CONTAINER; Type 0: Not a Combination Product 10/02/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 10/02/2017 Labeler - Johnson & Johnson Consumer Inc. (118772437)