PainFix Relief
- Product NDC
- 72749-001
- 11-digit product format
- 727490001
- Labeler code
- 72749
- Product ID
- 72749-001_90826319-b699-4480-9348-db2e2c9c45c1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- PainFix LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-02-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 50 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72749-001-00 | PainFix Relief | 1 in 1 BOX | GEL | 1 | | 4 |
| 72749-001-00 | PainFix Relief | 60 g in 1 TUBE | GEL | 60 | | 4 |
| 72749-001-03 | PainFix Relief | 57 g in 1 BOTTLE | GEL | 57 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72749-001 | PAINFIX RELIEF (MENTHOL) GEL [PAINFIX LLC] | 4 | Legacy NDC, 3 package rows | 20231230_4320db2b-69d0-421b-9890-eeb8c40318ec.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 |
|---|
| 72749-001-00 | 72749000100 | 1 TUBE in 1 BOX (72749-001-00) > 60 g in 1 TUBE | 1 tube | 2019-02-01 | 0000-00-00 | No | No | Current |
| 72749-001-03 | 72749000103 | 57 g in 1 BOTTLE | 57 g | | | | | Historical |