Label: NEUTROGENA OIL FREE ACNE STRESS CONTROL POWER CLEAR SCRUB- salicylic acid gel
- NDC Code(s): 69968-0073-4
- 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
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
-
Warnings
For external use only.
When using this product
- skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
- avoid contact with eyes. If contact occurs, flush thoroughly with water.
- Directions
- Other information
-
Inactive ingredients
Water, Cetyl Alcohol, PPG-15 Stearyl Ether, Microcrystalline Cellulose, Glycolic Acid, Glycerin, Polysorbate 60, Steareth-21, C12-15 Alkyl Lactate, Cetyl Lactate, Potassium Cetyl Phosphate, Microcrystalline Wax, Sodium Hydroxide, Xanthan Gum, Cocamidopropyl PG-Dimonium Chloride Phosphate, Fragrance, Disodium EDTA, Menthol, Benzalkonium Chloride, Camellia Sinensis Leaf Extract, Sodium Benzotriazolyl Butylphenol Sulfonate, Butylene Glycol, Cucumis Sativus (Cucumber) Fruit Extract, Chromium Hydroxide Green, Green 5, Yellow 5, Blue 1
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 125 mL Tube Label
-
INGREDIENTS AND APPEARANCE
NEUTROGENA OIL FREE ACNE STRESS CONTROL POWER CLEAR SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0073 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) CETYL ALCOHOL (UNII: 936JST6JCN) PPG-15 STEARYL ETHER (UNII: 1II18XLS1L) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) GLYCOLIC ACID (UNII: 0WT12SX38S) GLYCERIN (UNII: PDC6A3C0OX) STEARETH-21 (UNII: 53J3F32P58) POLYSORBATE 60 (UNII: CAL22UVI4M) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) CETYL LACTATE (UNII: A7EVH2RK4O) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) SODIUM HYDROXIDE (UNII: 55X04QC32I) XANTHAN GUM (UNII: TTV12P4NEE) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CUCUMBER (UNII: YY7C30VXJT) CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0073-4 125 mL in 1 TUBE; Type 0: Not a Combination Product 11/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 11/01/2016 Labeler - Johnson & Johnson Consumer Inc. (118772437)