Label: MICONAZOLE NITRATE- anti-fungal powder miconazole nitrate talc free powder
- NDC Code(s): 70000-0323-1
- Packager: LEADER/ Cardinal Health 110, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 21, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- clean the affected area and dry thoroughly
- apply a thin layer of product over affected area twice daily (morning and night) or as directed by a doctor
- supervise children in the use of this product
- for athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
- for athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks
- if conditions persist longer, consult a doctor
- this product is not effective on the scalp or nails
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
MICONAZOLE NITRATE
anti-fungal powder miconazole nitrate talc free powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0323 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 1.42 g in 71 g Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) CHLOROXYLENOL (UNII: 0F32U78V2Q) IMIDUREA (UNII: M629807ATL) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) TRICALCIUM PHOSPHATE (UNII: K4C08XP666) ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70000-0323-1 71 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 10/20/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 10/20/2017 Labeler - LEADER/ Cardinal Health 110, Inc. (063997360)