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Coralite Blue Ice

Medically reviewed on October 5, 2018

Dosage form: gel
Ingredients: MENTHOL .02g in 1g
Labeler: United Exchange Corp.
NDC Code: 65923-157

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                                                   Purpose

Menthol 2%........................................................Topical analgesic   

Uses

  • temporarily relieves minor aches and pains of muscles and joints associated with:
  • arthritis
  • simple backache 
  • strains
  • bruises
  • sport injuries
  • sprains
  • provides cooling penetrating relief

Warnings 

For external use only

Do not use

  • with other topical pain relievers
  • with heating pads or heating devices

When using this product

  • do not use in or near the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days
  • redness or irritation develops

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Clean affected area before applying product
  • 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: ask a doctor

Other information

  • store in a cool place
  • keep lid tightly closed
  • do not use, pour, spill or store near heat or open flame

Inactive ingredients

ammonium hydroxide, carbomer 940, cupric sulfate, FD&C blue no. 1, isopropyl alcohol, magnesium sulfate heptahydrate, purified water, sodium hydroxide, thymol

Distributed by:

United Exchange Corp.

17211 Valley View Ave.

Cerritos, CA 90703 U.S.A.

www.ueccorp.com

Toll Free: 1 800 814 8028

Made in China

CORALITE BLUE ICE 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-157
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL.02 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
AMMONIA 
CARBOMER 940 
CUPRIC SULFATE 
FD&C BLUE NO. 1 
ISOPROPYL ALCOHOL 
MAGNESIUM SULFATE HEPTAHYDRATE 
WATER 
SODIUM HYDROXIDE 
THYMOL 
Packaging
#Item CodePackage Description
1NDC:65923-157-27227 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/05/2016
Labeler - United Exchange Corp. (840130579)

 
United Exchange Corp.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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