Label: NEUTROGENA OIL FREE ACNE WASH PINK GRAPEFRUIT FOAMING SCRUB- salicylic acid gel
- NDC Code(s): 69968-0610-2, 69968-0610-4, 69968-0610-7
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 March 6, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Use
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Warnings
For external use only.
- Directions
- Other information
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Inactive ingredients
Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Microcrystalline Cellulose, Sodium Chloride, Acrylates Copolymer, Cellulose, Polysorbate 20, Fragrance, C12-15 Alkyl Lactate, Sodium Hydroxide, Disodium EDTA, Benzalkonium Chloride, Polyquaternium-7, Cocamidopropyl PG-Dimonium Chloride Phosphate, Sodium Benzotriazolyl Butylphenol Sulfonate, Propylene Glycol, Citrus Grandis (Grapefruit) Fruit Extract, Carrageenan, Agar, Ascorbyl Palmitate, Mica, Titanium Dioxide, Red 30, Red 40, Violet 2
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 198 mL Tube Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA OIL FREE ACNE WASH PINK GRAPEFRUIT FOAMING SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0610 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM CHLORIDE (UNII: 451W47IQ8X) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) POWDERED CELLULOSE (UNII: SMD1X3XO9M) POLYSORBATE 20 (UNII: 7T1F30V5YH) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PUMMELO (UNII: ET1TN5W71X) CARRAGEENAN (UNII: 5C69YCD2YJ) AGAR, UNSPECIFIED (UNII: 89T13OHQ2B) ASCORBYL PALMITATE (UNII: QN83US2B0N) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) D&C RED NO. 30 (UNII: 2S42T2808B) FD&C RED NO. 40 (UNII: WZB9127XOA) D&C VIOLET NO. 2 (UNII: 350KA7O6HK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0610-7 198 mL in 1 TUBE; Type 0: Not a Combination Product 12/30/2019 2 NDC:69968-0610-4 124 mL in 1 TUBE; Type 0: Not a Combination Product 12/30/2019 3 NDC:69968-0610-2 59 mL in 1 TUBE; Type 0: Not a Combination Product 12/09/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 12/09/2019 Labeler - Johnson & Johnson Consumer Inc. (118772437)