Label: NEKVNRO MULTI-PURPOSE TREATMENT- tolnaftate 1% multi-purpose treatment liquid

  • NDC Code(s): 84010-032-01, 84010-032-02
  • Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 24, 2024

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  • Active Ingredient

    Tolnaftate 1%

  • Purpose

    Antifungal

  • Use

    Cures most Athlete's Foot (Tinea Pedis)and Ringworm (Tinea Corporis).Relieves itching,scaling, cracking, burning, redness, sorenes, and irritation and discomfort. Helps prevent most athlete's foot(dermatophytosis) withdaily use.

  • Warnings

    For external use only.

  • Do not use

    on children under 2 years of age unless directed by a doctor.

  • When Using

    avoid contact with eyes.

  • Stop Use

    irritation occurs, there is no improvement within 4 weeks (for athlete's foot and ringworm).

  • Ask Doctor

    irritation occurs, there is no improvement within 4 weeks (for athlete's foot and ringworm).

  • Keep Oot Of Reach Of Children


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

  • Directions

    For athlete's foot and ring worm: use daily for 4 weeks. Clean the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Supervise child ren in the use of this product.This productis not effective for the prevention of ring worm of 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. To prevent athlete's foot, apply once or twice daily(morning and/or night).Apply to skin around the nail and cuticle.

  • Other information

    Store at room temperature 15-30℃(59-86)

  • Inactive ingredients

    water, euphorbia hirta whole, glycerin,hydracrylic acid,pseudolarix amabilis bark, resorcinol.

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    NEKVNRO MULTI-PURPOSE TREATMENT 
    tolnaftate 1% multi-purpose treatment liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84010-032
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    RESORCINOL (UNII: YUL4LO94HK)  
    EUPHORBIA HIRTA WHOLE (UNII: L13YF113GN)  
    HYDRACRYLIC ACID (UNII: C4ZF6XLD2X)  
    PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84010-032-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product09/24/2024
    2NDC:84010-032-0250 mL in 1 BOTTLE; Type 0: Not a Combination Product09/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00509/24/2024
    Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangxi Hemei Pharmaceutical Co., Ltd724892056manufacture(84010-032)