WALGREENS ICE BLUE GEL- menthol gel 
Walgreens Company

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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Walgreens Ice Blue Gel

Menthol 2%

Topical analgesic

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with

For external use only

Stop use and ask a doctor if:

Condition worsens, or if symptoms persist for more than 7 day or clear up and occur again withing a few days

If pregnant or breastfeeding

Ask a health professional before use

Keep out of reach of children

If swallowed get medical help or contact Poison Control Center (800-222-1222) right away

Directions

Other Information

Inactive Ingredients

Ammonium hydroxide, benzyl alcohol, carbopol 940, cupric sulphate, FD&C blue no.1, isopropyl alcohol, magnesium sulphate, PEG-40, hydrogenated castor oil, sodium hydroxide, thymol, water

Walgreens Ice Blue Gel

label

WALGREENS ICE BLUE GEL 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9621
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
THYMOL (UNII: 3J50XA376E)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CUPRIC SULFATE (UNII: LRX7AJ16DT)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
AMMONIA (UNII: 5138Q19F1X)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-9621-01226.8 g in 1 JAR; Type 0: Not a Combination Product04/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/01/2022
Labeler - Walgreens Company (008965063)
Establishment
NameAddressID/FEIBusiness Operations
ANICARE PHARMACEUTICALS PRIVATE LIMITED916837425manufacture(0363-9621)

Revised: 4/2022
Document Id: dd4120c9-dec0-704e-e053-2995a90acc23
Set id: cf5966f8-bd0b-2942-e053-2995a90a5cab
Version: 2
Effective Time: 20220422
 
Walgreens Company