Pain Crush
- Product NDC
- 69676-0004
- 11-digit product format
- 696760004
- Labeler code
- 69676
- Product ID
- 69676-0004_90140c05-4b61-f124-e053-2995a90a3a7f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Genexa Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-06-13
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 7 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 69676-0004-6 | Pain Crush | 89 mL in 1 BOTTLE, WITH APPLICATOR | GEL | 89 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69676-0004 | PAIN CRUSH (MENTHOL) GEL [GENEXA INC.] | 2 | Legacy NDC, 1 package rows | 20190814_6e8dd8bb-7204-34ca-e053-2a91aa0a9ef3.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 |
|---|
| 69676-0004-6 | 69676000406 | 89 mL in 1 BOTTLE, WITH APPLICATOR (69676-0004-6) | 89 ml | 2018-06-13 | 0000-00-00 | No | No | Current |