SUPER WHITE Stuff Pain Relief
- Product NDC
- 14448-307
- 11-digit product format
- 144480307
- Labeler code
- 14448
- Product ID
- 14448-307_09d7052e-ec52-ef60-e063-6294a90af214
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- BLUE SPRING WELLNESS, L.L.C.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-08-01
- 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
- SUPER WHITE Stuff 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 |
|---|
| 14448-307-50 | SUPER WHITE Stuff Pain Relief | 335 mL in 1 BOTTLE | CREAM | 335 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 14448-307 | SUPER WHITE STUFF PAIN RELIEF (MENTHOL) CREAM [BLUE SPRING WELLNESS, L.L.C.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231111_7779b26b-ae3b-4639-a6b0-826c7ab37a86.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 14448-307-50 | 14448030750 | 335 mL in 1 BOTTLE (14448-307-50) | 335 ml | 2020-08-01 | 0000-00-00 | No | No | Current |