Label: ANTIFUNGAL POWDER- tolnaftate aerosol, spray
- NDC Code(s): 55301-874-01
- Packager: ARMY & AIR FORCE EXCHANGE SERVICE
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 4, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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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 120°F. Intentional misuse by deliberately concentrating and inhaling contents can 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
- to prevent athlete's foot, apply once or twice daily (morning and/or night)
- 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 dail
- use daily for 4 weeks for athlete's foot and ringworm; use daily for 2 weeks
for jock itch
- if condition persists, consult a doctor
- this product is not effective on the scalp or nails
- if nozzle clogs, clean with a pin
- Other information
- Inactive ingredient
- Questions?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ANTIFUNGAL POWDER
tolnaftate aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55301-874 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength BHT (UNII: 1P9D0Z171K) ISOBUTANE (UNII: BXR49TP611) PPG-12-BUTETH-16 (UNII: 58CG7042J1) ALCOHOL (UNII: 3K9958V90M) KAOLIN (UNII: 24H4NWX5CO) ZEA MAYS (CORN) STARCH (UNII: O8232NY3SJ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55301-874-01 130 g in 1 CAN; Type 0: Not a Combination Product 01/03/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 01/03/2012 Labeler - ARMY & AIR FORCE EXCHANGE SERVICE (001695568)

