Label: ATHLETE FOOT TREATMENT KIT- terbinafine hydrochloride, tolnaftate kit

  • NDC Code(s): 85398-006-01, 85398-007-01, 85398-008-01
  • Packager: Beautivity LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 29, 2026

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Tolnaftate 1% (Soap Bar)

    Terbinafine Hydrochloride 1% (Cream)

  • PURPOSE

    antifungal

  • INDICATIONS & USAGE

    Soap Bar

    • Helps relieve and prevent itching, burning, cracking, and scaling associated with fungal infections such as athlete's foot, jock itch, ringworm, and other skin irritations.

    Cream

    • Cures most athlete's foot (tinea pedis)
    • Cures most jock itch (tinea cruris) and ringworm (tinea corporis)
    • Relieves itching, burning, cracking and scaling which accompany these conditions

  • WARNINGS

    For external use only

    • on children under 2 years of age unless directed by a doctor
    • on nails and scalp
    • in or near the mouth or eyes
    • for vaginal yeast infections

    When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor

    • If irritatioin occurs or there is no improvement within 2 weeks.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Soap Bar

    • Wash the affected area thoroughly
    • Allow Hermon Antifungal Soap to sit for 1-2 minutes before rinsing.
    • Dry the area completely after washing.

    Cream

    • 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

    Do not use if seal on tube is broken or is not visible. Store at room temperature. Protect from excessive heat (above 104°F / 40°C)

  • INACTIVE INGREDIENT

    Soap Bar
    Melaleuca Alternifolia (Tea Tree) Leaf Oil, Aqua (Water), Sorbitol, Elaeis Guineensis (Palm) Oil, Cocos Nucifera (Coconut) Oil, Olea Europaea (Olive) Fruit Oil, Propylene Glycol, Glycerin, Stearic Acid, Lauric Acid, Myristic Acid, Sodium Myristate, Sodium Glutamate, Sodium Hydroxide, Sodium Dodecylbenzene Sulfonate, Sulfur Thermal Water, Hamamelis Virginiana (Witch Hazel) Extract, Ceramide

    Inactive ingredients

    Cream
    Allantoin, Glycerin, Propylene Glycol, PCA Dimethicone, Ethylparaben, Glyceryl Stearate, Primary Alcohol Ethoxylate, Alumen, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexade- cane, Polysorbate 80, Aloe Barbadensis Leaf Juice, Parfum

  • QUESTIONS

    visit us at www.hermonhealth.com

  • PRINCIPAL DISPLAY PANEL

    kit

  • INGREDIENTS AND APPEARANCE
    ATHLETE FOOT TREATMENT KIT 
    terbinafine hydrochloride, tolnaftate kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85398-008
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85398-008-011 in 1 CARTON; Type 1: Convenience Kit of Co-Package08/20/2025
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 CARTON 60 g
    Part 21 CARTON 232 g
    Part 1 of 2
    ATHLETE FOOT CREAM 
    terbinafine hydrochloride cream
    Product Information
    Item Code (Source)NDC:85398-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TERBINAFINE HYDROCHLORIDE (UNII: 012C11ZU6G) (TERBINAFINE - UNII:G7RIW8S0XP) TERBINAFINE HYDROCHLORIDE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    POTASSIUM ALUM (UNII: 1L24V9R23S)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)  
    ALLANTOIN (UNII: 344S277G0Z)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    C12-15 PARETH-7 (UNII: 3XY03A79QH)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
    GLYCERYL STEARATE (UNII: 230OU9XXE4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85398-006-0160 g in 1 CARTON; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00508/18/2025
    Part 2 of 2
    ATHLETE FOOT MEDICATED BAR 
    tolnaftate soap
    Product Information
    Item Code (Source)NDC:85398-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM GLUTAMATE (UNII: W81N5U6R6U)  
    SORBITOL (UNII: 506T60A25R)  
    HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ELAEIS GUINEENSIS (PALM) OIL (UNII: 5QUO05548Z)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM MYRISTATE (UNII: 06BLC4V0IV)  
    SULFUR (UNII: 70FD1KFU70)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85398-007-01232 g in 1 CARTON; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00508/18/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00508/20/2025
    Labeler - Beautivity LLC (096573788)