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ARCTIC ICE pain relieving

Medically reviewed on February 24, 2017

Dosage form: gel
Ingredients: MENTHOL 2.0g in 100g
Labeler: Blue Cross Laboratories, Inc.
NDC Code: 22431-014

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.

ARCTIC ICE pain relieving gel

ARCTIC ICE ANALGESIC GEL

Active Ingredient

Menthol 2.0%

Purpose

Topical Analgesic

Uses

Temporary relief:

minor muscles aches and pains

Warnings

For external use only. Avoid contact with eyes.

Ask a doctor before use if you have cough associated with

  • smoking
  • excessive phlegm
  • asthma
  • emphysema
  • persistent or chronic cough

When using this product do not
  • heat
  • microwave
  • add to hot water or any container where healing water may cause splattering and result in burns
  • use in eyes or directly on mucous membranes
  • take by mouth or place in nostrils
  • apply to wounds or damaged skin
  • bandage skin

Consult a doctor and discontinue use

if condition worsens, persist for more than 1 week or tends to recur

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

For the temporary relief of minor muscle aches and pains

see important warnings under "When using this product"

  • not for use on children under 2 years of age
  • adults and children 2 years of age and older: apply to painful area and massage until gel is absorbed into the skin, repeat 3 to 4 times daily

Inactive Ingredients

blue 1, camphor, carbomer, isopropyl alcohol, methylchoroisothiazolinone, methuylisothiazoline, sodium hydroxide, water

ARCTIC ICE PAIN RELIEVING 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-014
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL2.0 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CAMPHOR (NATURAL) 
ALCOHOL 
FD&C BLUE NO. 1 
ISOPROPYL ALCOHOL 
METHYLCHLOROISOTHIAZOLINONE 
SODIUM HYDROXIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:22431-014-011 JAR in 1 PACKAGE
1227 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/23/2017
Labeler - Blue Cross Laboratories, Inc. (008298879)
Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd (530766098)
Establishment
NameAddressID/FEIOperations
Ningbo Liyuan Daily Chemical Products Co., Ltd530766098manufacture(22431-014)

 
Blue Cross Laboratories, Inc.

Further information

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

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