Label: NEUTROGENA OIL FREE ACNE STRESS CONTROL TRIPLE ACTION TONER- salicylic acid liquid
- NDC Code(s): 69968-0521-8
- 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 4, 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.
Flammable: Keep away from fire or flame.
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Directions
- cleanse skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
- Other information
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Inactive ingredients
Water, Alcohol Denat., Butylene Glycol, PPG-5-Ceteth-20, C12-15 Alkyl Lactate, Fragrance, Sodium Citrate, Cocamidopropyl PG-Dimonium Chloride Phosphate, PEG/PPG-20/6 Dimethicone, Sodium Hydroxide, Benzalkonium Chloride, Cetyl Lactate, Sodium Benzotriazolyl Butylphenol Sulfonate, Disodium EDTA, Camellia Sinensis Leaf Extract, Glycerin, Cucumis Sativus (Cucumber) Fruit Extract, Yellow 5, Blue 1, Green 5
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA OIL FREE ACNE STRESS CONTROL TRIPLE ACTION TONER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0521 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) ALCOHOL (UNII: 3K9958V90M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PPG-5-CETETH-20 (UNII: 4AAN25P8P4) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) PEG/PPG-20/6 DIMETHICONE (UNII: PWZ7N4UIKE) SODIUM HYDROXIDE (UNII: 55X04QC32I) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) CETYL LACTATE (UNII: A7EVH2RK4O) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) GREEN TEA LEAF (UNII: W2ZU1RY8B0) GLYCERIN (UNII: PDC6A3C0OX) CUCUMBER (UNII: YY7C30VXJT) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0521-8 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/01/2019 Labeler - Johnson & Johnson Consumer Inc. (118772437)