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Blue Ice by JMD All Star Impex Inc

Medically reviewed on May 30, 2018

Dosage form: gel
Ingredients: Menthol 2g in 100g
Labeler: JMD All Star Impex Inc
NDC Code: 51444-002

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.

Active Ingredient
Menthol 2.0%


Purpose
External pain reliever

Uses
Temporary relief of minor pains of muscles and joints associated with

  • Simple back ache
  • Arthritis
  • Sprains, strains or bruises

Warning
For external use only. Avoid contact with eyes



Do not use

  • Internally
  • With heating pads or devices
  • On wounds or damaged skin

Ask doctor before use if you have sensitive skin

When using this product
  • Use only as directed
  • Do not bandage tightly
  • Avoid contact with eyes and mucus membranes

If pregnant or breast feeding, ask a health professional before use

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately

Direction
  • Adult and children 2 years of age and older. Clean skin thoroughly. Apply liberally to affected area not more than 3-4 times daily. No protective cover needed.
  • May be used with ice packs
  • May be used with wet or dry bandage, but wrap loosely
  • Children under 2 years of age, consult a doctor

Other Information store between 59-85F (15-30C)
  • Keep tightly closed
  • Do not use, pour, spill or store near heat or open flames

Other Ingredients Carbomer 940, FDC Blue No. 1, Isopropyl Alcohol, Propylene Glycol, Purified Water, Sodium Hydroxide,

Package Label

BLUE ICE  
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51444-002
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol (Menthol) Menthol2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER TYPE C 
FD&C BLUE NO. 1 
ISOPROPYL ALCOHOL 
PROPYLENE GLYCOL 
WATER 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:51444-002-76216 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/15/2010
Labeler - JMD All Star Impex Inc (962316662)
Establishment
NameAddressID/FEIOperations
Steller Mercantile Pvt.Ltd.650493005manufacture

 
JMD All Star Impex Inc

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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