Label: ATHLETE FOOT CREAM- terbinafine hydrochloride cream
- NDC Code(s): 85398-006-01
- Packager: Beautivity LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 29, 2026
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
■ adults and children 12 years and over
■ use the tip of the cap to break the seal and open the tube
■ wash the affected skin with soap and water and dry completely before applying
■ for athlete’s foot wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.
■ between the toes only: apply twice a day (morning and night) for 1 week or as directed by a doctor
■ on the bottom or sides of the foot: apply twice a day (morning and night) for 2 weeks or as directed by a doctor
■ for jock itch and ringworm: apply once a day (morning or night) for 1 week or as directed by a doctor
■ wash hands after each use
■ children under 12 years: ask a doctor - OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ATHLETE FOOT CREAM
terbinafine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85398-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TERBINAFINE HYDROCHLORIDE (UNII: 012C11ZU6G) (TERBINAFINE - UNII:G7RIW8S0XP) TERBINAFINE HYDROCHLORIDE 1 g in 100 g Inactive Ingredients Ingredient Name Strength POTASSIUM ALUM (UNII: 1L24V9R23S) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL STEARATE (UNII: 230OU9XXE4) ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB) DIMETHICONE (UNII: 92RU3N3Y1O) C12-15 PARETH-7 (UNII: 3XY03A79QH) ALLANTOIN (UNII: 344S277G0Z) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ETHYLPARABEN (UNII: 14255EXE39) ISOHEXADECANE (UNII: 918X1OUF1E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85398-006-01 60 g in 1 CARTON; Type 0: Not a Combination Product 08/18/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 08/18/2025 Labeler - Beautivity LLC (096573788)

