Flexall Pain Relieving
- Product NDC
- 21695-642
- 11-digit product format
- 216950642
- Labeler code
- 21695
- Product ID
- 21695-642_79dd238d-87fe-4d89-bb3f-2677cae25993
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Rebel Distributors Corp
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1997-01-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 0 g/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-642-03 | Flexall Pain Relieving | 1 in 1 CARTON | GEL | 1 | | 1 |
| 21695-642-03 | Flexall Pain Relieving | 85 g in 1 TUBE | GEL | 85 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-642 | FLEXALL PAIN RELIEVING (MENTHOL) GEL [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20110211_79dd238d-87fe-4d89-bb3f-2677cae25993.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-642-03 | 21695064203 | 1 in 1 CARTON | Historical |