BLUESPRING Doctors Pain Formula Pain Relief
- Product NDC
- 83591-629
- 11-digit product format
- 835910629
- Labeler code
- 83591
- Product ID
- 83591-629_39e0ad70-7af0-cd09-e063-6394a90a0f22
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- ACA MANAGEMENT LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-07-07
- Substance
- MENTHOL
- Active strength
- 14 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BLUESPRING Doctors Pain Formula Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 14 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2391332 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83591-629-00 | BLUESPRING Doctors Pain Formula Pain Relief | 355 mL in 1 JAR | CREAM | 355 | | 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 |
|---|
| 83591-629-00 | 83591062900 | 355 mL in 1 JAR (83591-629-00) | 355 ml | 2025-07-07 | No | No | Current |