BM Berberis Vulgaris
- Product NDC
- 85816-5121
- Requested package NDC
- 85816-5121-1
- 11-digit product format
- 858165121
- Labeler code
- 85816
- Product ID
- 85816-5121_5ebffab5-95df-3f84-e063-6294a90af393
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Berberis Vulgaris
- Dosage form
- TINCTURE
- Route
- ORAL
- Labeler
- BM Private Limited
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-01
- Substance
- BERBERIS VULGARIS ROOT BARK
- Active strength
- 1 [hp_X]/mL
- 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 Berberis Vulgaris
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BERBERIS VULGARIS ROOT BARK | 1 [hp_X]/mL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85816-5121-1 | BM Berberis Vulgaris | 30 mL in 1 BOTTLE, GLASS | TINCTURE | 30 | 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 Berberis Vulgaris | BERBERIS VULGARIS | BM Private Limited | 38db12e8-d839-2f27-e063-6394a90a2f36 | 2025-07-01 | Warnings | 85816-5121-1 85816-5121 85816512101 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 85816-5121-1 | 85816512101 | 30 mL in 1 BOTTLE, GLASS (85816-5121-1) | 30 ml | 2015-01-01 | No | No | Current |