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#
Contacts and useful links#
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
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51316-997-04 | CVS Pain Relief | 85 g in 1 TUBE | GEL | 85 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- CVS Pain Relief
- Menthol 4%
- GLYCERIN
- DIMETHYL SULFONE
- GREEN TEA LEAF
- TROLAMINE
- ISOPROPYL ALCOHOL
- MENTHOL
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
- ARNICA MONTANA
- ALOE VERA LEAF
- PHENOXYETHANOL
- WATER
- CAMPHOR (SYNTHETIC)
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51316-997 | 51316-997-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| DIMETHYL SULFONE | 9H4PO4Z4FT | IACT |
| GREEN TEA LEAF | W2ZU1RY8B0 | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) | 59TL3WG5CO | IACT |
| ARNICA MONTANA | O80TY208ZW | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| WATER | 059QF0KO0R | IACT |
| CAMPHOR (SYNTHETIC) | 5TJD82A1ET | 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 4% | CVS | d1660d55-1ee0-7aa2-e053-2995a90a6579 | 2024-12-11 | Warnings | 51316-997-04 51316-997 51316099704 28f15d7e-f9cc-4807-e063-6294a90ab6f7 d1660d55-1ee0-7aa2-e053-2995a90a6579 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
