Label: BUNION PAIN RELIEF CREAM cream

  • NDC Code(s): 83675-019-01
  • Packager: Guangzhou Hanhai Trading Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 7, 2023

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

View All Sections
  • Active Ingredient

    Ginger 12.0%

  • Purpose

    Relieve Pain

  • Use

    Help relieve pain

  • Warnings

    For external use only.

    Keep Out Of Reach Of Children
    Pregnant, breast-feeding, people with severe chronic diseases or allergic to the raw materials are forbidden to use

  • 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

    After cleaning .take appropriate gel evenlyon

  • Other information

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

    Avoid direct sunlight

  • Inactive ingredients

    Mint
    Camphor

  • PRINCIPAL DISPLAY PANEL

    01

  • INGREDIENTS AND APPEARANCE
    BUNION PAIN RELIEF CREAM 
    bunion pain relief cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83675-019
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER12 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    MINT (UNII: FV98Z8GITP)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83675-019-0120 g in 1 BOX; Type 0: Not a Combination Product10/07/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/07/2023
    Labeler - Guangzhou Hanhai Trading Co., Ltd (419707381)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Hanhai Trading Co., Ltd419707381label(83675-019) , manufacture(83675-019)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!