Label: DAILY CLEANSER SALICYLIC ACID ACNE TREATMENT- salicylic acid gel
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Contains inactivated NDC Code(s)
NDC Code(s): 58876-101-14, 58876-101-18 - Packager: DR LIN SKINCARE
- 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 June 17, 2013
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- ASK DOCTOR/PHARMACIST
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
INACTIVE INGREDIENTS
Water, Sodium Laureth Sulfate, Sodium Cocoamphoacetate, Glycerin, Lauryl Glucoside, Sodium Cocoyl Glutamate, Sodium Lauryl Glucose Carboxylate, Arbutin, Kojic Acid, Ascorbic Acid, Sodium PCA, Allantoin, Panthenol, PEG-150 Distearate, Phenoxyethanol, Aminomethyl Propanol, Methylisothiazolinone, Fragrance
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INGREDIENTS AND APPEARANCE
DAILY CLEANSER SALICYLIC ACID ACNE TREATMENT
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58876-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674) GLYCERIN (UNII: PDC6A3C0OX) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG) SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL) ARBUTIN (UNII: C5INA23HXF) KOJIC ACID (UNII: 6K23F1TT52) ASCORBIC ACID (UNII: PQ6CK8PD0R) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) ALLANTOIN (UNII: 344S277G0Z) PANTHENOL (UNII: WV9CM0O67Z) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) PHENOXYETHANOL (UNII: HIE492ZZ3T) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58876-101-18 240 mL in 1 BOTTLE 2 NDC:58876-101-14 120 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/13/2013 Labeler - DR LIN SKINCARE (622329980) Establishment Name Address ID/FEI Business Operations Westwood Laboratories Inc. 069926483 manufacture(58876-101) , pack(58876-101)