DIGITALIS PUR
- Product NDC
- 15631-2718
- 11-digit product format
- 156312718
- Labeler code
- 15631
- Product ID
- 15631-2718_19ba75a8-51ad-c9f5-e063-6394a90a5214
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIGITALIS PUR
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-05-23
- Substance
- DIGITALIS
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F1T8QT9U8B | DIGITALIS | 8031-42-3 | DIGITALIS |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 15631-2718-0 | 15631271800 | 10 mL in 1 BOTTLE (15631-2718-0) | 10 ml | 2024-05-23 | No | No | Historical |
| 15631-2718-1 | 15631271801 | 30 mL in 1 BOTTLE (15631-2718-1) | 30 ml | 2024-05-23 | No | No | Historical |