Label: JOCK ITCH POWDER- miconazole nitrate powder
- NDC Code(s): 56104-901-71
- Packager: Premier Brands of America Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 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 the 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
JOCK ITCH POWDER
miconazole nitrate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56104-901 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) SODIUM BICARBONATE (UNII: 8MDF5V39QO) ALLANTOIN (UNII: 344S277G0Z) TRICALCIUM PHOSPHATE (UNII: K4C08XP666) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) STARCH, CORN (UNII: O8232NY3SJ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56104-901-71 71 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 06/01/2023 Labeler - Premier Brands of America Inc (063849780)