Label: NEUTROGENA DEEP CLEAN PURIFYING COOLING GEL SCRUB- salicylic acid gel
- NDC Code(s): 69968-0740-4
- 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 January 14, 2023
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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 final part333D 10/01/2017 Labeler - Johnson & Johnson Consumer Inc. (118772437)