Label: MENTHOL- maximum strength medicated foot powder talc free powder
- NDC Code(s): 36800-252-10
- Packager: Topco Associates LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 31, 2023
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INGREDIENTS AND APPEARANCE
MENTHOL
maximum strength medicated foot powder talc free powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:36800-252 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2.8 g in 283 g Inactive Ingredients Ingredient Name Strength ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8) TRICALCIUM PHOSPHATE (UNII: K4C08XP666) EUCALYPTUS OIL (UNII: 2R04ONI662) SODIUM BICARBONATE (UNII: 8MDF5V39QO) BENZETHONIUM CHLORIDE (UNII: PH41D05744) PEPPERMINT OIL (UNII: AV092KU4JH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36800-252-10 283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/10/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 02/10/2019 Labeler - Topco Associates LLC (006935977)