Label: MICONAZOLE FOOT POWDER- miconazole powder
- NDC Code(s): 42669-073-01
- Packager: Davion, Inc.
- Category: HUMAN OTC DRUG LABEL
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 December 13, 2022
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- Active Ingredients
For external use only.
Stop use and ask a doctor if
- condition worsens
- symptoms last more than 7 days or clear up and occur again within a few days
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
MICONAZOLE FOOT POWDER
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42669-073 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 2 g in 100 g Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) IMIDUREA (UNII: M629807ATL) TRICALCIUM PHOSPHATE (UNII: K4C08XP666) ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8) ALLANTOIN (UNII: 344S277G0Z) CHLOROXYLENOL (UNII: 0F32U78V2Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42669-073-01 78 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/19/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 08/19/2022 Labeler - Davion, Inc. (174542928)