Label: GOOD NEIGHBOR PHARMACY THERAPEUTIC BLUE- menthol gel

  • NDC Code(s): 24385-225-40
  • Packager: AmerisourceBergen Drug Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 22, 2015

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

  • Drug Facts

    Active Ingredients

    Active ingredient

    Menthol 2%

  • PURPOSE

    pain relieving gel

  • Uses

    for the temporary relief of minor aches and

    pains of muscles and joints associated with

    • simple backache • arthritis • strains

    • bruises • sprains

  • warnings

    For external use only

    when using this product

    • avoid contact with the eyes

    • do not bandage tightly

    • do not apply to wounds or damaged skin

    • do not use with heating pads or other heating devices

    Stop using and ask a doctor if

    • condition worsens, or if symptoms persist for more

    than 7 days or clear up and occur again within a

    few days

    Keep out of the reach of children

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

  • Directions

    • adults and children 2 years of age and older: apply

    to affected area not more than 3 to 4 times daily

    • children under 2 years of age: do not use, consult a doctor

  • Inactive Ingredients

    Ammonium Hydroxide, Carbomer, Cupric Sulfate, FD&C Blue No. 1,

    Isopropyl Alcohol, Magnesium Sulfate,

    Sodium Hydroxide, Thymol, Water.

  • SPL UNCLASSIFIED SECTION

    This product is not manufactured by Novartis Consumer

    Health, Inc., owner of the registered trademark Mineral Ice®.

  • PRINCIPAL DISPLAY PANEL

    Untitled.jpg

  • INGREDIENTS AND APPEARANCE
    GOOD NEIGHBOR PHARMACY THERAPEUTIC BLUE 
    menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-225
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIA (UNII: 5138Q19F1X)  
    CARBOMER 934 (UNII: Z135WT9208)  
    CUPRIC SULFATE (UNII: LRX7AJ16DT)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    MAGNESIUM SULFATE (UNII: DE08037SAB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    THYMOL (UNII: 3J50XA376E)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24385-225-40227 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34803/11/1988
    Labeler - AmerisourceBergen Drug Corporation (007914906)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg, LLC927768135manufacture(24385-225) , label(24385-225)