Label: WALGREENS ICE BLUE GEL- menthol gel

  • 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 April 22, 2022

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  • ACTIVE INGREDIENT

    Menthol 2%

  • PURPOSE

    Topical analgesic

  • Uses

    Temporarily relieves minor aches and pains of muscles and joints associated with

    • simple backache
    • arthritis
    • strains
    • bruises
    • sprains
  • WARNINGS

    For external use only

  • WHEN USING

    • Do not use with other topical pain relievers
    • Do not use with heating pads or other heating devices
    • Avoid contact with eyes
    • Do not bandage tightly
    • Do not apply to wounds or damage skin
  • Stop use and ask a doctor if:

    Condition worsens, or if symptoms persist for more than 7 day or clear up and occur again withing a few days

  • If pregnant or breastfeeding

    Ask a health professional before use

  • Keep out of reach of children

    If swallowed get medical help or contact Poison Control Center (800-222-1222) right away

  • Directions

    • Clean affected area before applying product
    • Adults and children 2 years and older, apply to the affected area not more than 3 to 4 times daily
    • Children under 2 years of age, ask a doctor before using this product
  • Other Information

    • Do not freeze
    • Store at room temperatiure
    • Keep container tightly closed when not in use
    • do not use, pour, spill or store near heat or open flame
  • Inactive Ingredients

    Ammonium hydroxide, benzyl alcohol, carbopol 940, cupric sulphate, FD&C blue no.1, isopropyl alcohol, magnesium sulphate, PEG-40, hydrogenated castor oil, sodium hydroxide, thymol, water

  • Walgreens Ice Blue Gel

    label

  • INGREDIENTS AND APPEARANCE
    WALGREENS ICE BLUE GEL 
    menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9621
    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
    THYMOL (UNII: 3J50XA376E)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CUPRIC SULFATE (UNII: LRX7AJ16DT)  
    MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
    AMMONIA (UNII: 5138Q19F1X)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9621-01226.8 g in 1 JAR; Type 0: Not a Combination Product04/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34804/01/2022
    Labeler - Walgreens Company (008965063)
    Establishment
    NameAddressID/FEIBusiness Operations
    ANICARE PHARMACEUTICALS PRIVATE LIMITED916837425manufacture(0363-9621)
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