Label: DERMAN ANTIFUNGAL- tolnaftate aerosol, powder
- NDC Code(s): 54312-230-01
- Packager: Compania Internacional de Comercio, S.A.P.I. de C.V.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 5, 2026
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Uses
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Warnings
For external use only
Flammable: Contents under pressure. Do not puncture or incinetare or store at a temperature above 120°F. Use only as directed. Intentional misuse by deliberately concentrating and inhaling aerosol products can be harmful or fatal. Do not use near flame or spark or white smoking.
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Directions
• clean the affected area and dry thoroughly
• shake can well before use: hold can about 6 inches from the area to be treated
• apply a thin layer over the affected area twice daily (morning and night), or as directed by a doctor
• supervise children in the use of this product
• use daily for 4 weeks for athlete's foot and ringworm; use daily for 2 weeks for jock itch
• to prevent most athlete's foot apply once or twice daily (morning and/or night)
• if condition persists longer, consult a doctor
• this product is not effective on the scalp or nails
• 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 - Other information
- Inactive ingredients
- Questions or comments?
- Package Labeling:
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INGREDIENTS AND APPEARANCE
DERMAN ANTIFUNGAL
tolnaftate aerosol, powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54312-230 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 ALCOHOL (UNII: 3K9958V90M) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) STARCH, CORN (UNII: O8232NY3SJ) ISOBUTANE (UNII: BXR49TP611) KAOLIN (UNII: 24H4NWX5CO) PPG-12-BUTETH-16 (UNII: 58CG7042J1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54312-230-01 130 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/13/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 11/13/2025 Labeler - Compania Internacional de Comercio, S.A.P.I. de C.V. (822165213) Registrant - Compania Internacional de Comercio, S.A.P.I. de C.V. (822165213)
