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
- DEA Schedule: None
- Marketing Status: OTC monograph not 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.
Updated July 20, 2021
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- Active ingredient
For external use only.
Stop and consult a doctor if
- conditions worsens
- symptoms persists for more than 7 days or clear up and occur again within a few days
- Inactive ingredients
- Principal Display Panel
INGREDIENTS AND APPEARANCE
maximum strength medicated foot powder talc free powder
Product 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 SODIUM BICARBONATE (UNII: 8MDF5V39QO) BENZETHONIUM CHLORIDE (UNII: PH41D05744) PEPPERMINT OIL (UNII: AV092KU4JH) EUCALYPTUS OIL (UNII: 2R04ONI662) ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8) TRICALCIUM PHOSPHATE (UNII: K4C08XP666) 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)