Label: KROGER DAILY FACE WASH- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 30142-729-07 - Packager: THE KROGER COMPANY
- 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 September 24, 2014
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- ACTIVE INGREDIENT
- USES
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WARNINGS
FOR EXTERNAL USE ONLY
- DIRECTIONS
- OTHER INFORMATION
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INACTIVE INGREDIENTS
WATER, GLYCEIRN, MYRISTIC ACID, STEARIC ACID, SODIUM LAUROYL SARCOSINATE, PALMITIC ACID, POTASSIUM HYDROXIDE, LAURIC ACID, POLYQUATERNIUM-10, FRAGRANCE, TETRASODIUM EDTA, PENTASODIUM PENTETATE, TETRASODIUM ETIDRONATE, MENTHOL, ALOE BARBADENSIS LEAF JUICE, MALTODEXTRIN, POTASSIUM SORBATE, SODIUM BENZOATE, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN
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- LABEL COPY
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INGREDIENTS AND APPEARANCE
KROGER DAILY FACE WASH
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-729 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) GLYCERIN (UNII: PDC6A3C0OX) MYRISTIC ACID (UNII: 0I3V7S25AW) STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) PALMITIC ACID (UNII: 2V16EO95H1) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) LAURIC ACID (UNII: 1160N9NU9U) POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS) EDETATE SODIUM (UNII: MP1J8420LU) PENTASODIUM PENTETATE (UNII: 961TOZ5L7T) ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4) MENTHOL (UNII: L7T10EIP3A) ALOE VERA LEAF (UNII: ZY81Z83H0X) MALTODEXTRIN (UNII: 7CVR7L4A2D) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-729-07 184 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 09/22/2014 Labeler - THE KROGER COMPANY (006999528) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(30142-729)