Label: NEUTROGENA DEEP CLEAN PURIFYING COOLING GEL SCRUB- salicylic acid gel
- NDC Code(s): 69968-0740-4
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
- Directions
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Other information
Sunburn Alert
This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterwards. Store at room temperature.
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Inactive ingredients
Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Cellulose Sorbitol, Acrylates Crosspolymer-4, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Polysorbate 20, Glycolic Acid, Fragrance, Microcrystalline Wax, Sodium Hydroxide, Menthol, Disodium EDTA, Ferric Ferrocyanide, Green 3
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 119 g Tube Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA DEEP CLEAN PURIFYING COOLING GEL SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0740 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) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) POWDERED CELLULOSE (UNII: SMD1X3XO9M) SORBITOL (UNII: 506T60A25R) POLYSORBATE 20 (UNII: 7T1F30V5YH) GLYCOLIC ACID (UNII: 0WT12SX38S) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) SODIUM HYDROXIDE (UNII: 55X04QC32I) FERRIC FERROCYANIDE (UNII: TLE294X33A) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0740-4 119 g in 1 TUBE; Type 0: Not a Combination Product 10/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 10/01/2017 Labeler - Kenvue Brands LLC (118772437)