Label: IBEALEE NALI LIQUID liquid

  • NDC Code(s): 83675-029-01
  • Packager: Guangzhou Hanhai Trading Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 12, 2023

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  • Active Ingredient

    Tolnaftate 1%

  • Purpose

    Anti-fungal

  • Use

    for relief and treatment of pain,
    soreness, and inflammation from nail
    fungus. Symptoms:

    ■discolored nails
    ■brittle nails

    ■distorted nails

  • Warnings

    For external use only. Some individuals may be sensitive to essential oils. Begin with a small drop to determine if product causes any irritation. Discontinue use if any irritation occurs. Stop use and consult a doctor if condition worsens. Not for use on children under the age of 2 without physician direction.

  • Do not use

    If you feel uncomfortable, please stop using it

  • When Using

    Use after cleansing skin

  • Ask Doctor

    ask doctor in case of Sensitive Skin

  • Keep Oot Of Reach Of Children

    If pregnant or breast-feeding, ask a
    health professional before use. If
    accidental ingestion and adverse
    reaction occurs, get medical help or
    contact a Poison Control Center.

  • Directions

    shake well before use.
    Wash and thoroughly dry the affected
    area. Apply 1-2 drops and gently rub
    into affected area three times per day.
    Wash hands after applying.

  • Other information

    *Keep in cool dark place
    *Store upright
    *Tighten cap after use to prevent
    oxidation

  • Inactive ingredients

    Water,Lonicerae Japonicae flos,Angelicae,Glycerin, Allantoin, Garlic Extract, Tea Tree Oil.

  • PRINCIPAL DISPLAY PANEL

    010203

  • INGREDIENTS AND APPEARANCE
    IBEALEE NALI LIQUID 
    ibealee nali liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83675-029
    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
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GARLIC (UNII: V1V998DC17)  
    ALLANTOIN (UNII: 344S277G0Z)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)  
    ANGELICA SINENSIS ROOT (UNII: B66F4574UG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83675-029-0120 mL in 1 BOTTLE; Type 0: Not a Combination Product11/12/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00511/12/2023
    Labeler - Guangzhou Hanhai Trading Co., Ltd (419707381)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Hanhai Trading Co., Ltd419707381manufacture(83675-029) , label(83675-029)
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