Label: MAXIMUM STRENGTH MEDICATED FOOT POWDER- medicated foot powder powder
- NDC Code(s): 11673-510-10
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 13, 2024
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INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH MEDICATED FOOT POWDER
medicated foot powder powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-510 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.1 g in 1 g Inactive Ingredients Ingredient Name Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) EUCALYPTUS OIL (UNII: 2R04ONI662) ACACIA (UNII: 5C5403N26O) PEPPERMINT OIL (UNII: AV092KU4JH) SODIUM BICARBONATE (UNII: 8MDF5V39QO) TALC (UNII: 7SEV7J4R1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-510-10 283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/30/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/30/2013 Labeler - Target Corporation (006961700)