CVS ULTRA STRENGTH PAIN RELIEVING- menthol patch 
CVS Pharmacy, 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 5%                                                             Topical Analgesic

Uses Temporarily relieves minor pain associated with:

Warnings

For external use only

When using this product

Stop use and ask a doctor if

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

Other information

Inactive ingredients butylated hydroxytoluene, carboxymethylcellulose sodium, caster oil, concentrated glycerin, EDTA-2Na, gelatin, isopropyl myristate, kaolin, magnesium aluminium hydroxide, methylparaben, polyacrylic acid, polysorbate 80, polyvinyl alcohol, purified water, sodium polyacrylate, sorbitan monooleate, tartaric acid, titanium dioxide

Distributed By:

CVS Pharmacy, Inc.

One CVS Drive.

Woonsocket, RI 02895

Made in Korea

image description

CVS ULTRA STRENGTH PAIN RELIEVING 
menthol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-476
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL750 mg
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
CASTOR OIL (UNII: D5340Y2I9G)  
GELATIN (UNII: 2G86QN327L)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
KAOLIN (UNII: 24H4NWX5CO)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
POLYVINYL ALCOHOL (UNII: 532B59J990)  
WATER (UNII: 059QF0KO0R)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
TARTARIC ACID (UNII: W4888I119H)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-476-041 in 1 CARTON
15 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34809/20/2013
Labeler - CVS Pharmacy, Inc. (062312574)

Revised: 12/2015
Document Id: c380eb3c-2081-479e-9a36-13e22e2b82e0
Set id: 87816ca3-140f-47bb-bb08-20305972cc16
Version: 2
Effective Time: 20151203
 
CVS Pharmacy, Inc.