Label: MULTI VITAMIN ACNE CLEARING- salicylic acid lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 70367-013-02, 70367-013-05 - Packager: Only Yourx, 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 23, 2020
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- ACTIVE INGREDIENT
- PURPOSE
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Water, Butylene Glycol, Cetyl Ethylhexanoate, Glyceryl Stearate, PEG-100 Stearate, Stearic Acid, Cetyl Alcohol, Magnesium Aluminum Silicate, Tetrahexyldecyl Ascorbate (Vitamin C), Retinol (Vitamin A), Willow Bark Extract, Panthenol, Bisabolol, Tocopheryl Acetate (Vitamin E Acetate), Witch Hazel Extract, Sage Extract, Dimethicone, Caprylic/Capric Triglyceride, Sodium Edetate, Potassium Sorbate, Aminomethyl Propanol, Xanthan Gum, Ethylhexylglycerin, Phenoxyethanol
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INGREDIENTS AND APPEARANCE
MULTI VITAMIN ACNE CLEARING
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70367-013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1.5 g in 100 mL Inactive Ingredients Ingredient Name Strength COBALT DISODIUM EDETATE (UNII: 3EY1Y2QRLI) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETYL ETHYLHEXANOATE (UNII: 134647WMX4) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) PEG-100 STEARATE (UNII: YD01N1999R) STEARIC ACID (UNII: 4ELV7Z65AP) CETYL ALCOHOL (UNII: 936JST6JCN) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) RETINOL (UNII: G2SH0XKK91) WILLOW BARK (UNII: S883J9JDYX) PANTHENOL (UNII: WV9CM0O67Z) .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WITCH HAZEL (UNII: 101I4J0U34) SAGE (UNII: 065C5D077J) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9) AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70367-013-02 59.15 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/26/2014 2 NDC:70367-013-05 14.8 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/26/2014 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 08/26/2014 Labeler - Only Yourx, Inc. (089207519)
