CVS Pain Relief Colorless Gel

Manufacturer
CVS
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:42:35

Label at a glance#

ProductCVS Pain Relief
Active ingredientMENTHOL
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

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

arthritis

backache

strains

sprains

WARNINGS SECTION

For external use only

Flammable: Keep away from excessive heat or open flame

OTC - ASK DOCTOR SECTION

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.

OTC - WHEN USING SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
415974menthol 4 % Topical GelPSN3
415974menthol 0.04 MG/MG Topical GelSCD3
415974menthol 4 % Topical GelSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-997-04CVS Pain Relief85 g in 1 TUBEGEL853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51316-997CVS PAIN RELIEF (MENTHOL 4%) GEL [CVS]3Current NDC, Legacy NDC, 1 package rows20241213_d1660d55-1ee0-7aa2-e053-2995a90a6579.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-99751316-997-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CVS Pain ReliefMENTHOL 4%CVSd1660d55-1ee0-7aa2-e053-2995a90a65792024-12-11WarningsExact identifier
ndc (package): 51316-997-04
ndc (product): 51316-997
ndc11 (package): 51316099704
spl id: 28f15d7e-f9cc-4807-e063-6294a90ab6f7
spl set id: d1660d55-1ee0-7aa2-e053-2995a90a6579

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.