EQUALINE BLUE ICE PAIN RELIEVING - menthol gel 
SUPERVALU INC

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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Drug Facts

Active Ingredient                                                                       Purpose

Menthol 2.0% ..........................................................................Topical Analgesic

Uses: Temporary relief of minor aches and pains in: Muscles and joints.

Warnings:

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

When using this product do not:

To do so may result in excessive skin irritation or skin burn.

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product

and consult a physician.  If you have sensitive skin, consult a physician.  If skin irritation develops, discontinue use and seek the advice of a physician before

using this product.

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

Directions:

Inactive Ingredients: Aqua (water), Isopropyl Alcohol, Carbomer, Thymol, Ammonium Hydroxide, Sodium Hydroxide, Magnesium Sulfate, FD and C Blue No.1

DISTRIBUTED BY SUPERVALU INC.

EDEN PRAIRIE, MN 55344 USA

MADE IN CANADA

image of carton labelEnter section text here

EQUALINE BLUE ICE PAIN RELIEVING 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-488
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
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
THYMOL (UNII: 3J50XA376E)  
AMMONIA (UNII: 5138Q19F1X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41163-488-32227 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34810/03/2011
Labeler - SUPERVALU INC (006961411)

Revised: 10/2011
Document Id: 4025f145-dc24-488e-a079-c5ac79992cfc
Set id: 7a652b7c-662d-4605-814d-86cf5084797f
Version: 1
Effective Time: 20111003
 
SUPERVALU INC