Label: CLEAN AND CLEAR DUAL ACTION MOISTURIZER- salicylic acid lotion
- NDC Code(s): 69968-0589-4
- 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 5, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- clean the 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, Dicaprylyl Ether, Cetearyl Alcohol, Glycerin, Neopentyl Glycol, Diethylhexanoate, Dimethicone, Methyl Gluceth-20, Menthyl Lactate, Aluminum Starch Octenylsuccinate, Ceteth-10 Phosphate, Dicetyl Phosphate, Steareth-20, Steareth-2, Neopentyl Glycol Diisostearate, Fragrance, Sodium Hydroxide, Hydrogenated Lecithin, Xanthan Gum, Magnesium Aluminum Silicate, Disodium EDTA, BHT, Titanium Dioxide
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label
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INGREDIENTS AND APPEARANCE
CLEAN AND CLEAR DUAL ACTION MOISTURIZER
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0589 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DICAPRYLYL ETHER (UNII: 77JZM5516Z) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) DIMETHICONE (UNII: 92RU3N3Y1O) METHYL GLUCETH-20 (UNII: J3QD0LD11P) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) STEARETH-20 (UNII: L0Q8IK9E08) STEARETH-2 (UNII: V56DFE46J5) NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW) SODIUM HYDROXIDE (UNII: 55X04QC32I) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) XANTHAN GUM (UNII: TTV12P4NEE) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0589-4 118 mL in 1 BOTTLE, PUMP; 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)