Label: PED X CALLUS REMOVERS, EXTRA THICK MEDICATED- salicylic acid patch
PED X CALLUS REMOVERS, MEDICATED- salicylic acid patch
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Contains inactivated NDC Code(s)
NDC Code(s): 60193-400-01, 60193-400-02, 60193-401-01, 60193-401-02 - Packager: Pacific World Corporation
- 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 October 17, 2014
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- wash affected area and dry thoroughly.
- if necessary, cut medicated disk to fit callus before applying.
- after 48 hours remove the medicated disk.
- repeat this procedure every 48 hours as needed for up to 14 days (until callus is removed).
- may soak callus in warm water for 5 minutes to assist in removal.
- Other information
- Inactive ingredient
- Questions?
- PRINCIPAL DISPLAY PANEL - 4 mg Patch Cello Pack - Extra Thick
- PRINCIPAL DISPLAY PANEL - 4 mg Patch Cello Pack - Medicated
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INGREDIENTS AND APPEARANCE
PED X CALLUS REMOVERS, EXTRA THICK MEDICATED
salicylic acid patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60193-401 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic acid (UNII: O414PZ4LPZ) (Salicylic acid - UNII:O414PZ4LPZ) Salicylic acid 4 mg Inactive Ingredients Ingredient Name Strength Vinyl acetate (UNII: L9MK238N77) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60193-401-02 4 in 1 CELLO PACK 1 NDC:60193-401-01 1 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 09/01/2007 PED X CALLUS REMOVERS, MEDICATED
salicylic acid patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60193-400 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic acid (UNII: O414PZ4LPZ) (Salicylic acid - UNII:O414PZ4LPZ) Salicylic acid 4 mg Inactive Ingredients Ingredient Name Strength Vinyl acetate (UNII: L9MK238N77) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60193-400-02 4 in 1 CELLO PACK 1 NDC:60193-400-01 1 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 09/01/2007 Labeler - Pacific World Corporation (089693097)