Label: MICONAZOLE NITRATE- athletes foot liquid spray
- NDC Code(s): 0363-4208-53
- Packager: Walgreens Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 9, 2024
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- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Extremely flammable:
Do not use while smoking or near heat or flame. Do not puncture or incinerate, contents under pressure. Do not store at temperature above 120ºF.
When using this product
- avoid contact with the eyes or mouth
- use only as directed
Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal.
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Directions
- wash affected area and dry thoroughly
- shake can well and spray a thin layer 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, consult a doctor
- this product is not effective on the scalp or nails
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
MICONAZOLE NITRATE
athletes foot liquid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-4208 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 3 g in 150 g Inactive Ingredients Ingredient Name Strength ACETONE (UNII: 1364PS73AF) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALCOHOL (UNII: 3K9958V90M) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-4208-53 150 g in 1 CAN; Type 0: Not a Combination Product 05/18/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 05/18/2010 Labeler - Walgreens Company (008965063)