Label: WALGREENS OIL-FREE ACNE WASH- salicylic acid solution
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-0536-11 - Packager: Walgreens 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 January 10, 2014
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- Active ingredient
- Purpose
- Indications
- Warnings
- Keep Out of Reach of Children.
- Directions
- Other Information
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Inactive ingredients
sodium C14-16 olefin sulfonate, water, cocamidopropyl betaine, propylene glycol, fragrance, PEG-80 sorbitan laurate, C12-15 alkyl lactate, yellow 5, cocamidopropyl PG-dimonium chloride phosphate, benzalkonium chloride, chamomilla recutita (matricaria) flower extract, aloe barbadensis leaf juice, disodium EDTA, red 40
Distributed by: Walgreen Co.
200 Wilmot Rd., Deerfield, IL 60015
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©2012 Walgreen Co.Manufactured in Israel
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INGREDIENTS AND APPEARANCE
WALGREENS OIL-FREE ACNE WASH
salicylic acid solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0536 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 SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITAN MONOLAURATE (UNII: 6W9PS8B71J) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) CHAMOMILE (UNII: FGL3685T2X) ALOE VERA LEAF (UNII: ZY81Z83H0X) EDETATE DISODIUM (UNII: 7FLD91C86K) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0536-11 269 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 01/05/2013 Labeler - Walgreens Company (008965063)