CVS Pain Relief
- Product NDC
- 51316-161
- 11-digit product format
- 513160161
- Labeler code
- 51316
- Product ID
- 51316-161_23aaba32-8d1b-6a5b-e063-6394a90a3adc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol 4%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- CVS
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-11-15
- Substance
- MENTHOL, (+)-
- Active strength
- 4 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CVS Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, (+)- | 4 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C6B1OE8P3W |
| Rxcui | 415974 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51316-161-02 | CVS Pain Relief | 74 mL in 1 BOTTLE, PLASTIC | GEL | 74 | | 2 |
| 51316-161-03 | CVS Pain Relief | 89 mL in 1 TUBE | GEL | 89 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51316-161 | CVS PAIN RELIEF (MENTHOL 4%) GEL [CVS] | 2 | Current NDC, 2 package rows | 20241116_20234356-5e80-b79e-e063-6294a90a2ee3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51316-161-02 | 51316016102 | 74 mL in 1 BOTTLE, PLASTIC (51316-161-02) | 74 ml | 2024-11-15 | No | No | Current |
| 51316-161-03 | 51316016103 | 89 mL in 1 TUBE (51316-161-03) | 89 ml | 2024-11-15 | No | No | Current |