BM Digitalis Purpurea
- Product NDC
- 85816-5106
- Requested package NDC
- 85816-5106-1
- 11-digit product format
- 858165106
- Labeler code
- 85816
- Product ID
- 85816-5106_5c56cf6e-7266-7848-e063-6294a90ab347
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Digitalis Purpurea
- Dosage form
- GLOBULE
- Route
- ORAL
- Labeler
- BM Private Limited
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-01
- Substance
- DIGITALIS
- Active strength
- 30 [hp_C]/1000mg
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BM Digitalis Purpurea
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIGITALIS | 30 [hp_C]/1000mg |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85816-5106-1 | BM Digitalis Purpurea | 30000 mg in 1 BOTTLE, GLASS | GLOBULE | 30000 | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| BM Digitalis Purpurea | DIGITALIS PURPUREA | BM Private Limited | 38dfb441-b08a-b6a8-e063-6394a90a72ef | 2025-07-01 | Warnings | 85816-5106-1 85816-5106 85816510601 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 85816-5106-1 | 85816510601 | 30000 mg in 1 BOTTLE, GLASS (85816-5106-1) | 30000 mg | 2015-01-01 | No | No | Current |