CVS PAIN RELIEF- menthol 4% gel 
CVS

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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CVS Pain Relief Colorless Gel

Menthol 4%

Topical Analgesic

Temporary relief from minor aches and pains of sore muscles and joints associated with:

arthritis

backache

strains

sprains

For external use only

Flammable: Keep away from excessive heat or open flame

Ask a doctor before use if you have: sensitive skin

Stop use and ask a doctor if

condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days.

When using this product

Use only as directed

Avoid contact with eyes or mucous membranes

Do not apply to wounds or damaged skin

Do not use with other ointments, creams, sprays or liniments

Do not apply to irritated skin or if excessive irritation develops

Do not bandage or use with heating pad or device

Store in a cool dry place away from direct sunlight

Wash hands after use with cool water

If pregnant or breastfeeding, ask a health professional before use

Keep out of reach of children: If accidentally ingested, get medical help or contact a poison Control immediately (1800-222-1222)

Directions

Adults and children 2 years of age and older: Rub a thin film over affected areas not more than daily: massage not necessary

Children under 2 years of age : Consult physician

Aloe Barbadensis Leaf Juice, Arnica Montana Flower Extract, Camellia Sinensis Leaf Extract, Camphor, Carbomer, Dimethyl Sulphone (MSM), Glycerin, Isopropyl Alcohol, Phenoxyethanol, Triethanolamine, Water

Package Label

CVS PAIN RELIEF 
menthol 4% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-997
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
TROLAMINE (UNII: 9O3K93S3TK)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
ARNICA MONTANA (UNII: O80TY208ZW)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51316-997-0485 g in 1 TUBE; Type 0: Not a Combination Product09/29/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34809/29/2020
Labeler - CVS (062312574)

Revised: 9/2022
Document Id: e9c2924b-e204-f6b9-e053-2995a90a2f09
Set id: d1660d55-1ee0-7aa2-e053-2995a90a6579
Version: 2
Effective Time: 20220928
 
CVS