Label: MICONAZOLE NITRATE- athletes foot powder spray talc free aerosol, powder
- NDC Code(s): 63868-180-46
- Packager: Chain Drug Marketing Association
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
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WARNINGS
For external use only.
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
- do not get into 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)
- 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
- use daily for 4 weeks for athlete's foot and ringworm; use daily for 2 weeks for jock itch, if conditions persist, consult a doctor
- this product is not effective on the scalp or nails
- in case clogging, clear nozzle under running water
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
MICONAZOLE NITRATE
athletes foot powder spray talc free aerosol, powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-180 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 2.6 g in 130 g Inactive Ingredients Ingredient Name Strength ISOBUTANE (UNII: BXR49TP611) KAOLIN (UNII: 24H4NWX5CO) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) ALCOHOL (UNII: 3K9958V90M) ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-180-46 130 g in 1 CAN; Type 0: Not a Combination Product 12/19/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 12/19/2017 Labeler - Chain Drug Marketing Association (011920774)