Label: WALGREENS MEDICATED CALLUS REMOVERS- salicylic acid disc
- NDC Code(s): 0363-0819-01
- Packager: WALGREENS Co.
- 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 March 3, 2023
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
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INGREDIENTS AND APPEARANCE
WALGREENS MEDICATED CALLUS REMOVERS
salicylic acid discProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0819 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 17.67 mg in 44.18 mg Inactive Ingredients Ingredient Name Strength POLYVINYL ALCOHOL (UNII: 532B59J990) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) VINYL ACETATE (UNII: L9MK238N77) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0819-01 1 in 1 CONTAINER 06/01/2013 1 4 in 1 CELLO PACK 1 44.18 mg in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358F 06/01/2013 Labeler - WALGREENS Co. (008965063) Registrant - PEDIFIX, INC. (122271935) Establishment Name Address ID/FEI Business Operations PEDIFIX 122271935 pack(0363-0819) , label(0363-0819) Establishment Name Address ID/FEI Business Operations AKRON 186569323 manufacture(0363-0819)