24 7 Relief and Recovery Pain Relieving
- Product NDC
- 87656-964
- 11-digit product format
- 876560964
- Labeler code
- 87656
- Product ID
- 87656-964_50acffaf-7b87-df5e-e063-6394a90ad6b5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Triplicare Inc
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-13
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 37 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 24 7 Relief and Recovery Pain Relieving
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 37 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 1655936 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87656-964-04 | 24 7 Relief and Recovery Pain Relieving | 118 mL in 1 TUBE | CREAM | 118 | | 1 |
| 87656-964-32 | 24 7 Relief and Recovery Pain Relieving | 946 mL in 1 BOTTLE | CREAM | 946 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87656-964-04 | 87656096404 | 118 mL in 1 TUBE (87656-964-04) | 118 ml | 2026-04-13 | No | No | Current |
| 87656-964-32 | 87656096432 | 946 mL in 1 BOTTLE (87656-964-32) | 946 ml | 2026-04-13 | No | No | Current |