CVS Pain Relief Spray

Manufacturer
CVS
Effective date
2025-03-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:15:10

Label at a glance#

ProductCVS Pain Relief
Active ingredientMENTHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.5%

OTC - PURPOSE SECTION

Topical analgesic

INDICATIONS & USAGE SECTION

Temporary relief from minor aches 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 flames. Contents Under Pressure.

Do Not Puncture Or Incinerate

Do Not Store At Temperature Above 120°F

OTC - ASK DOCTOR SECTION

Ask a Doctor before using if you have sensitive skin

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

Do not bandage

Do not use with heating pad or device

Store in a cool dry place away from sunlight

Wash hands after use with cool water

OTC - STOP USE SECTION

Stop use and ask doctor if condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222)

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Spray on to the affected areas not more than 4 times daily; message not necessary

Children under 12 years of age: Consult physician

INACTIVE INGREDIENT SECTION

Aloe Barbadensis leaf Juice, Arnica Montana Flower Extract, Camellia Sinensis Leaf Extract, Dimethyl Sulphone (MSM), Isobutane, Propylene Glycol, SD Alcohol 40 B (30%), Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4.5 oz label4.5 oz labelPackage LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489073menthol 10.5 % Topical SprayPSN4
1489073menthol 105 MG/ML Topical SpraySCD4
1489073menthol 10.5 % Topical SpraySY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-996-04CVS Pain Relief128 g in 1 BOTTLE, SPRAYSPRAY1284
51316-996-10CVS Pain Relief85 g in 1 BOTTLE, SPRAYSPRAY854

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-99651316-996-10, 51316-996-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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 10.5%CVSd0ea80ce-38b2-acde-e053-2995a90a47e52025-03-31WarningsExact identifier
ndc (package): 51316-996-04
ndc (package): 51316-996-10
ndc (product): 51316-996
ndc11 (package): 51316099604
ndc11 (package): 51316099610
spl id: 2a8a4561-b693-5cee-e063-6394a90a89e3
spl set id: d0ea80ce-38b2-acde-e053-2995a90a47e5

Reported adverse events (FAERS/openFDA)#

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