Label: NEKVNRO MEDICATED LIP OINTMENT.- medicated lip ointment ointment

  • NDC Code(s): 84844-004-01, 84844-004-02
  • Packager: Guoyu Trading Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 30, 2024

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  • Active Ingredient

    Camphor 2%

  • Purpose

    External Analgesic

  • Use

    ·Helps provide relief of symptoms of cold sores and dry lips.

  • Warnings

    ·For external use only. When using this product, keep out of eyes. Rinse with water to remove.

  • Do not use

    on deep puncture wounds, serious burns, or animal bites.

  • When Using

    this product, keep out of eyes. Rinse with water to remove.

  • Stop Use

    if the condition worsens or symptoms last more than 7 days or clear up and occur again within a few days

  • Ask Doctor

    if the condition worsens or symptoms last more than 7 days or clear up and occur again within a few days

  • Keep Oot Of Reach Of Children

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

  • Directions

    · Apply to lips not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.

  • Other information

    This is a personal care item and should be used by one individual only.Inactive

  • Inactive ingredients

    ·Beeswax white, GLYCERYL 2-CAPRYLATE，Lanolin, Oleamide, Paraffin,Propyl Acetate

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    NEKVNRO MEDICATED LIP OINTMENT. 
    medicated lip ointment ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84844-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN (UNII: 7EV65EAW6H)  
    PROPYL ACETATE (UNII: 4AWM8C91G6)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    GLYCERYL 2-CAPRYLATE (UNII: O8TCW8DUW8)  
    OLEAMIDE (UNII: 7L25QK8BWO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84844-004-0110 g in 1 TUBE; Type 0: Not a Combination Product10/31/2024
    2NDC:84844-004-0220 g in 1 TUBE; Type 0: Not a Combination Product10/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/31/2024
    Labeler - Guoyu Trading Co., Ltd. (963348600)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guoyu Trading Co., Ltd.963348600manufacture(84844-004)
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