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Blue Ice Analgesic

Dosage form: gel
Ingredients: Menthol 2.0g in 100g
Labeler: Delon Laboratories (1990) Ltd
NDC Code: 61734-021

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 Facts

Active Ingredient / Purpose
Menthol 2.0%

    Temporary relief of minor aches and pains in
  • muscles and joints

  • Put a small amount onto your palms and rub hands together until dry.

  • For external use only. Avoid contact with eyes and mucous membranes.


When using this product do not:

  • use with heating pads or heating devices
  • use, pour, spill, or store near open flame
  • use with other creams, sprays or liniments
  • apply to damaged skin or wounds - Bandage area tightly
To do so may result in excessive skin irritation or skin burn.

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

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. If you have sensitive skin consult a physician. If skin irritation develops, discontinue use and seek the advice of a physician before using this product.


  • See important warnings under when using this product
  • Do not apply to children under 2 years of age, unless advised by a physician.
  • Adults and children over 2 years and older: Apply liberally to painful area and massage until gel is absorbed into the skin. Repeat 3 to 4 times daily.

Inactive Ingredients ‚ÄčDeinoized Water, Isopropyl Alcohol, Carbomer, Thymol, Ammonium Hydroxide, Sodium Hydroxide, Magnesium sulfate, FDC Blue 1


menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61734-021
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol (Menthol) Menthol2.0 g  in 100 g
Product Characteristics
FlavorImprint Code
#Item CodePackage Description
1NDC:61734-021-01100 g in 1 BOTTLE, PUMP
2NDC:61734-021-02113.56 g in 1 CONTAINER
3NDC:61734-021-03227 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34805/07/2010
Labeler - Delon Laboratories (1990) Ltd (248364184)

Revised: 07/2010
Delon Laboratories (1990) Ltd

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.