Label: UP AND UP DUAL EFFECTS MOISTURIZER- salicylic acid lotion
- NDC Code(s): 11673-931-53
- Packager: TARGET CORPORATION
- 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 October 3, 2022
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
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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 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, Glycerin, Cetearyl Alcohol, Dimethicone, Neopentyl Glycol Diisostearate, Neopentyl Glycol Diethylhexanoate, Aluminum Starch Octenylsuccinate, Methyl Gluceth-20, Dicetyl Phosphate, Ceteth-10 Phosphate, Mentyl Lacatate, Steareth-21, Steareth-2, Fragrance, Xanthan Gum, Disodium EDTA, Sodium Hydroxide, Magnesium Aluminum Silicate, BHT.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
UP AND UP DUAL EFFECTS MOISTURIZER
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-931 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 STEARETH-2 (UNII: V56DFE46J5) GLYCERIN (UNII: PDC6A3C0OX) DICAPRYLYL ETHER (UNII: 77JZM5516Z) WATER (UNII: 059QF0KO0R) STEARETH-21 (UNII: 53J3F32P58) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) EDETATE DISODIUM (UNII: 7FLD91C86K) METHYL GLUCETH-20 (UNII: J3QD0LD11P) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) SODIUM HYDROXIDE (UNII: 55X04QC32I) XANTHAN GUM (UNII: TTV12P4NEE) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-931-53 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/11/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 10/11/2012 Labeler - TARGET CORPORATION (006961700)