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Blue Ice Analgesic

Dosage form: gel
Ingredients: MENTHOL 2g 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


Menthol 2.0%

Purpose

Topical Analgesic

Uses


Temporary relief of minor aches and pains in muscles and joints

Warnings

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

When using this product do not:

heat
microwave
add to hot water or any container where heating wate
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

Stop use and ask a physician if:

condition worsens
symptoms persist for more than 7 days or clear up and occur again within a few days
skin irritation develops
hypersensitivity develops

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

if you have sensitive skin, ask a health professional before use.

Directions

  • 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.

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

Inactive Ingredients

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

Adults and children 2 years of age and older:

  • apply liberally to painful area and massage until gel is absorbed
  • use up to 304 times daily or as directed by a doctor

Delon 8oz (227g)

delon 100g pump

Penetro 227g

BLUE ICE ANALGESIC 
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 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
THYMOL 
AMMONIA 
SODIUM HYDROXIDE 
MAGNESIUM SULFATE 
FD&C BLUE NO. 1 
WATER 
ISOPROPYL ALCOHOL 
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) 
Product Characteristics
ColorblueScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#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 not finalpart34805/07/2010
Labeler - Delon Laboratories (1990) Ltd (248364184)
Establishment
NameAddressID/FEIOperations
Delon Laboratories (1990) Inc.243387722manufacture(61734-021), pack(61734-021), label(61734-021)

Revised: 11/2016
 
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.

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