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#
Contacts and useful links#
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
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51316-996-04 | CVS Pain Relief | 128 g in 1 BOTTLE, SPRAY | SPRAY | 128 | 4 | |
| 51316-996-10 | CVS Pain Relief | 85 g in 1 BOTTLE, SPRAY | SPRAY | 85 | 4 |
Products#
Every source-derived product name is available through these pages.
- CVS Pain Relief
- Menthol 10.5%
- MENTHOL
- GREEN TEA LEAF
- WATER
- DIMETHYL SULFONE
- DEHYDRATED ALCOHOL
- PROPYLENE GLYCOL
- ISOBUTANE
- GLYCERIN
- ALOE VERA LEAF
- ARNICA MONTANA
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51316-996 | 51316-996-10, 51316-996-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL | L7T10EIP3A | ACTIB |
| GREEN TEA LEAF | W2ZU1RY8B0 | IACT |
| WATER | 059QF0KO0R | IACT |
| DIMETHYL SULFONE | 9H4PO4Z4FT | IACT |
| DEHYDRATED ALCOHOL | 3K9958V90M | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| ISOBUTANE | BXR49TP611 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| ARNICA MONTANA | O80TY208ZW | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| CVS Pain Relief | MENTHOL 10.5% | CVS | d0ea80ce-38b2-acde-e053-2995a90a47e5 | 2025-03-31 | Warnings | 51316-996-04 51316-996-10 51316-996 51316099604 51316099610 2a8a4561-b693-5cee-e063-6394a90a89e3 d0ea80ce-38b2-acde-e053-2995a90a47e5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

