Pain Relief
- Product NDC
- 69396-175
- 11-digit product format
- 693960175
- Labeler code
- 69396
- Product ID
- 69396-175_4cc58afa-6dae-b9db-e063-6394a90a23c8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Trifecta Pharmaceuticals USA, LLC.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-25
- Substance
- MENTHOL
- Active strength
- 10.5 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pain Relief
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 10.5 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 1489073 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69396-175-03 | Pain Relief | 89 mL in 1 BOTTLE, SPRAY | SPRAY | 89 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69396-175-03 | 69396017503 | 89 mL in 1 BOTTLE, SPRAY (69396-175-03) | 89 ml | 2026-01-25 | No | No | Current |