Label: NEUTROGENA ACNE PROOFING DAILY SCRUB- salicylic acid gel
- NDC Code(s): 69968-0112-4
- 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 June 6, 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
- Other information
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Inactive ingredients
Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Sorbitol Cellulose, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Acrylates Crosspolymer-4, Panthenol, Sodium Hydroxide, Fragrance, Microcrystalline Wax, C12-15 Alkyl Lactate, Benzalkonium Chloride, Disodium EDTA, Cocamidopropyl PG-Dimonium Chloride Phosphate, Talc, Yellow 5 Lake, Red 30
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 119 g Tube Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA ACNE PROOFING DAILY SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0112 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 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) SORBITOL (UNII: 506T60A25R) POWDERED CELLULOSE (UNII: SMD1X3XO9M) PANTHENOL (UNII: WV9CM0O67Z) SODIUM HYDROXIDE (UNII: 55X04QC32I) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) D&C RED NO. 30 (UNII: 2S42T2808B) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) TALC (UNII: 7SEV7J4R1U) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0112-4 119 g in 1 TUBE; Type 0: Not a Combination Product 10/01/2017 05/22/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 10/01/2017 05/22/2024 Labeler - Johnson & Johnson Consumer Inc. (118772437)