Label: HERMON ATHLETES FOOT TOLNAFTATE 1% KIT- tolnaftate 1% kit kit

  • NDC Code(s): 85398-007-02, 85398-017-02, 85398-018-01
  • 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

    • Soap Bar: Tolnaftate 1%
    • Cream: Tolnaftate 1%
  • PURPOSE

    Antifungal

  • DOSAGE & ADMINISTRATION

    • cures most athlete's foot (tinea pedis)
    • cures most jock itch(tinea cruris) and ringworm (tinea corporis)
    • relieves itching, burning, cracking and scaling which accomppany these conditions
    • For effective relief of itching, cirritation, redness, scaling, cracking, burning, soreness, anddiscomfort which can accompany these conditions.
  • WARNINGS

    For external use only

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

    avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    if irritation occurs or there is no improvement within 2 wveeks.

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

  • INDICATIONS & USAGE

    Directions (Cream)

    • adults and children 12 years and over
    • use the tip of thecap to break the seal and open the tube
    • wash the affedted 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 ttoes only: apply twice a day (morning and night) for 1 week or as directed by a doctor
    • on the bottom or sides ofthe foot: apply twice a day (morning and night) for 2 weeks or as directed by a doctor
    • for jock itch and ringworm: apply oncea 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
    • wash affected area and dry thoroughly
    • apply a thin layer over affected area twice daily (morning and night)
    • supervise children in the use of this product
    • use daily for2 weeks


    Directions (Soap Bar)

    • Wet skin with warm water and lather soap.
    • Gently massage onto affeected areas.
    • Rinse thoroughly and dry.
    • Use twice daily or as directed by 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

    Cream:

    Allantoin, Glycerin, Propylene Glycol, PCA Dimethicone, Ethylparaben, Glyc Ethoxylate, Alumen, Sodium Acrylate/Sodium Acryloyldimethyl Taurrate Copolymer, Isohexadecane, Polysorbate 80, Aloe Barbadensis Leaf Juice

    Soap Bar:

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

  • QUESTIONS

    visit us at www.hermonhealth.com

  • PRINCIPAL DISPLAY PANEL

    package

  • INGREDIENTS AND APPEARANCE
    HERMON ATHLETES FOOT TOLNAFTATE 1% KIT 
    tolnaftate 1% kit kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85398-018
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85398-018-011 in 1 CARTON; Type 1: Convenience Kit of Co-Package10/31/2025
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 TUBE 57 g
    Part 20 CARTON 1 g  in 116 
    Part 1 of 2
    INITIAL DRUG LISTING - HERMON ATHLETES FOOT 1% TOLNAFTATE CREAM 
    tolnaftate 1% cream
    Product Information
    Item Code (Source)NDC:85398-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE0.57 g  in 57 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)  
    ALCOHOL (UNII: 3K9958V90M)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    GLYCERYL STEARATE (UNII: 230OU9XXE4)  
    DIMETHICONE 6 (UNII: RB8V8W9FQN)  
    ALLANTOIN (UNII: 344S277G0Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    POTASSIUM ALUM (UNII: 1L24V9R23S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85398-017-0257 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00510/31/2025
    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) TOLNAFTATE1.16 g  in 116 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SODIUM GLUTAMATE (UNII: W81N5U6R6U)  
    SODIUM MYRISTATE (UNII: 06BLC4V0IV)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    SORBITOL (UNII: 506T60A25R)  
    MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)  
    OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ELAEIS GUINEENSIS (PALM) OIL (UNII: 5QUO05548Z)  
    SULFUR (UNII: 70FD1KFU70)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85398-007-02116 g in 1 CARTON; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00510/31/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00510/31/2025
    Labeler - Beautivity LLC (096573788)
    Registrant - Beautivity LLC (096573788)