Label: ZEASORB- miconazole nitrate powder
- NDC Code(s): 0316-0231-25, 0316-0232-25
- Packager: Crown Laboratories
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 15, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use (Athlete's Foot)
- Use (Jock Itch)
- Warnings
-
Directions (Athlete's Foot)
- 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
- pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
- use daily for 4 weeks
- if condition persists longer, consult a doctor
- this product is not effective on the scalp or nails
-
Directions (Jock Itch)
- 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
- use daily for 2 weeks
- if condition persists longer, consult a doctor
- this product is not effective on the scalp or nails
- Other information
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ZEASORB
miconazole nitrate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0316-0232 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 SODIUM ACRYLATES CROSSPOLYMER-2 (UNII: D3HPR4WW6F) ALDIOXA (UNII: 8T66I31YNK) CHLOROXYLENOL (UNII: 0F32U78V2Q) IMIDUREA (UNII: M629807ATL) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) Product Characteristics Color white (white to off-white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0316-0232-25 71 g in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2018 04/16/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 03/14/2011 04/16/2025 ZEASORB
miconazole nitrate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0316-0231 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 ALDIOXA (UNII: 8T66I31YNK) CHLOROXYLENOL (UNII: 0F32U78V2Q) IMIDUREA (UNII: M629807ATL) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM ACRYLATES CROSSPOLYMER-2 (UNII: D3HPR4WW6F) Product Characteristics Color white (white to off-white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0316-0231-25 71 g in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2018 03/31/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 03/14/2011 03/31/2025 Labeler - Crown Laboratories (079035945)