ARCTIC ICE ANALGESIC- menthol gel 
Blue Cross Labs

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.

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Arctic Ice Analgesic Gel

Active Ingredient:               Purpose

Menthol, 1%  .................. Topical analgesic

Uses: temporarily relieves:

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

Consult a doctor and discontinue use;

if conditon worsens, persists for more than 1 week or tends to recur

Warnings: For external use only; avoid contact with eyes. Ask a doctor before use if you have associated with

When using this product, do; heat

Directions:

For the temporary relief of minor muscle aches and pains. See important warnings under "When using this product"

Blue 1, Camphor, Carbomer, Isopropyl Alcohol, Methylchoroisothiazolinone, Methylisothiazolinone, Sodium Hydroxide, Water.

Arctic Ice

Analgesic Gel

NET WT. 8 OZ. (227)

image description

ARCTIC ICE ANALGESIC 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-600
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22431-600-01227 g in 1 JAR; Type 0: Not a Combination Product09/16/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34109/16/2015
Labeler - Blue Cross Labs (008298879)
Registrant - Blue Cross Labs (008298879)
Establishment
NameAddressID/FEIBusiness Operations
Blue Cross Labs008298879manufacture(22431-600)

Revised: 1/2017
Document Id: 267b7d9d-34f5-487b-a40b-f1043e2fa4cd
Set id: 81ddb5ad-8068-4669-8e48-9d1a66e44ef5
Version: 4
Effective Time: 20170127
 
Blue Cross Labs