Label: TOLNAFATE- tolnaftate powder spray aerosol, spray
- NDC Code(s): 83324-234-46
- Packager: Chain Drug Marketing Association
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 9, 2026
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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WARNINGS
For external use only.
Extremely Flammable:
Keep away from fire, sparks, and heated surfaces.
Contents under pressure.Do not puncture or incinerate. Do not store at
temperature above 120ºF.
When using this product
- avoid spraying in eyes
- use only as directed
- intentional misuse by deliberately concentrating and inhaling the 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 of the product over affected area twice daily (morning and night) or as directed by a doctor
- to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily ( morning and/or 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
- for athlete's foot and ringworm: use daily for 4 weeks; for jock itch, use daily for 2 weeks
- if condition persists, 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
TOLNAFATE
tolnaftate powder spray aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-234 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 ZEA MAYS (CORN) STARCH (UNII: O8232NY3SJ) BHT (UNII: 1P9D0Z171K) PPG-12-BUTETH-16 (UNII: 58CG7042J1) ISOBUTANE (UNII: BXR49TP611) KAOLIN (UNII: 24H4NWX5CO) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-234-46 130 g in 1 CAN; Type 0: Not a Combination Product 04/10/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 04/10/2025 Labeler - Chain Drug Marketing Association (011920774)
