Label: HC MAX FOR JOCK ITCH- tolnaftate ointment

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 29, 2023

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

  • ACTIVE INGREDIENT


    Active IngredientPurpose
    Tolnaftate 1%Anti-fungal
  • INDICATIONS & USAGE

    Uses ■ Proven clinically effective in the treatment of most jock itch (tinea cruris). ■ For effective relief of itching, burning, or chafing associated with jock itch.

  • Warnings

    For external use only.

  • DO NOT USE

    Do not use on children under 2 years of age unless directed by a doctor.

  • WHEN USING

    When using this product ■ avoid contact with eyes.

  • STOP USE

    Stop use and ask a doctor if ■ Irritation occurs. ■ There is no improvement within 2 weeks.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN. In case of accidental ingestion, contact a physician, emergency medical care facility or Poison Control Center immediately for advice.

  • DOSAGE & ADMINISTRATION

    Directions ■ Clean the affected area with soap and warm water and dry thoroughly. ■ Apply a thin layer of HC Max™ Anti-Fungal Ointment over affected area twice daily (morning and night) or as directed by a doctor. ■ Supervise children in the use of this product. ■ For jock itch, use daily for 2 weeks. ■ If condition persists longer, consult a doctor. ■ This product is not effective on the scalp or nails.

  • STORAGE AND HANDLING

    Other information Store at controlled room temperature 15°-30°C (59°-86°F) Do not permit to freeze.

  • INACTIVE INGREDIENT

    Inactive ingredients
    Aloe Vera Leaf, Carbomer Homopolymer Type A (Allyl Pentaerythritol Crosslinked), Dimethicone 350, Eucalyptol, Glyceryl Monostearate,  Lavender Oil, Olive Oil, Phenoxyethanol, Poloxamer 188, Purified Water (USP), Sodium Hydroxide,  Tea Tree Oil.

  • QUESTIONS

    Questions? 1-800-824-4894

  • PRINCIPAL DISPLAY PANEL

    HC MAX™

    Anti-Fungal Ointment
    Ungüento Anti-Hongos

    Tolnaftate 1%


    FOR
    JOCK ITCH


    Clinically Proven to
    CURE Most Jock Itch

    Probado Clínicamente para Curar
    La Mayoria de Casos de
    Tiña Inguinal


    plus
    Aloe & Tea Tree Oil
    for skin health

    CLINICALLY PROVEN INGREDIENT

    Relives
    ✓ Itching  
    ✓ Burning
     
    ✓ Scaling
    ✓ Chafing

    Alivia
    ✓ Picazón 
    ✓ Ardor
    ✓ Descamación

    ✓ Agrietamientó 

    NET WT 1 OZ (28g)

    Probado Clínicamente
    para Curar
    La Mayoria de
    Casos de Tiña
    Inguinal


    más
    Aloe y aceite de árbol de té
    para la salud de la piel

    HC MAX™
    Ungüento anti-hongos

    es infundido con 5 aceites
    naturales que incluyen
    árbol de té, eucalipto,
    aloe, oliva y lavanda.

    KRAMER
    LABORATORIES

    Distributed by:
    Kramer Laboratories, Inc.
    Bridgewater, NJ 08807
    kramerlabs.com
    funginail.com
    1-800-824-4894

    K0220

    carton

    KRAMER
    LABORATORIES


    Kramer Laboratories, Inc. Bridgewater, NJ 08807 1-800-824-4894

    Maximum Strength / Máxima Potencia

    HC MAX™ FOR JOCK ITCH

    Anti-Fungal Ointment / Ungüento Anti-Hongos
    Tolnaftate 1%


    NET CONTENT 1 OZ. (28 G)

    K0220

    label
  • INGREDIENTS AND APPEARANCE
    HC MAX FOR JOCK ITCH 
    tolnaftate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55505-194
    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
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Carbomer Homopolymer Type A (Allyl Pentaerythritol Crosslinked) (UNII: F68VH75CJC)  
    Dimethicone 350 (UNII: 2Y53S6ATLU)  
    Eucalyptol (UNII: RV6J6604TK)  
    Glyceryl Monostearate (UNII: 230OU9XXE4)  
    Lavender Oil (UNII: ZBP1YXW0H8)  
    Olive Oil (UNII: 6UYK2W1W1E)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Poloxamer 188 (UNII: LQA7B6G8JG)  
    Water (UNII: 059QF0KO0R)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Tea Tree Oil (UNII: VIF565UC2G)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55505-194-261 in 1 CARTON06/01/2020
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00506/01/2020
    Labeler - Kramer Laboratories (122720675)