Label: NECK HUMP REMOVAL PATCH patch

  • NDC Code(s): 83675-008-01
  • Packager: Guangzhou Hanhai Trading Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated September 20, 2023

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  • Active Ingredient

    Ceramic Powder 21.0%

  • Purpose

    Quick Pain Relief

  • Use

    Neck Hump Removal Patch to help quick relieve pain

  • Warnings

    For external use only. Do not take it internally.

    Keep Out Of Reach Of Children
    Prohibited for those with damaged skin.

  • Do not use

    Product shall not be eat

  • When Using

    Do not stick around eyes and mouth,This product cannot replace drugs.

  • Stop Use

    In case of adverse reactions, please stop using this product.If the symptoms.

  • Ask Doctor

    ask doctor in case of adverse reactions

  • Keep Oot Of Reach Of Children

    Keep Out Of Reach Of Children

  • Directions

    Take one piece of this product when needed, remove the waxpaper,

    stick to the desired area and press the surrounding, replace it every day.

    Children should be used under adult supervision.

  • Other information

    Store the product in a cool, dry and well-ventilated place

    Avoid direct sunlight

  • Inactive ingredients

    base liner

    substrate

    release paper

    pressure-sensitive adhesive

  • PRINCIPAL DISPLAY PANEL

    01

  • INGREDIENTS AND APPEARANCE
    NECK HUMP REMOVAL PATCH 
    neck hump removal patch patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83675-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IVERMECTIN (UNII: 8883YP2R6D) (IVERMECTIN - UNII:8883YP2R6D) IVERMECTIN14 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    LINERIXIBAT (UNII: 386012Z45S)  
    5-BROMO-4-CHLORO-3-INDOLYL PHOSPHATE (UNII: BZ64NZV99J)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    DIETHYLENE GLYCOL ABIETATE (UNII: CXM0P78DR3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83675-008-018 in 1 BAG; Type 0: Not a Combination Product09/19/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/19/2023
    Labeler - Guangzhou Hanhai Trading Co., Ltd (419707381)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Hanhai Trading Co., Ltd419707381label(83675-008) , manufacture(83675-008)
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