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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DIGITALIS PUR
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIGITALIS | 6 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F1T8QT9U8B |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 15631-2718-0 | DIGITALIS PUR | 10 mL in 1 BOTTLE | LIQUID | 10 | | 1 |
| 15631-2718-1 | DIGITALIS PUR | 30 mL in 1 BOTTLE | LIQUID | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 15631-2718 | DIGITALIS PUR LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC] | 1 | Current NDC, 2 package rows | 20240601_19ba912f-cd86-4cca-e063-6294a90a233b.zip |
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |
| 15631-2718-1 | 15631271801 | 30 mL in 1 BOTTLE (15631-2718-1) | 30 ml | 2024-05-23 | No | No | Current |