BMNP BELLIS PERENNIS
- Product NDC
- 82969-5242
- 11-digit product format
- 829695242
- Labeler code
- 82969
- Product ID
- 82969-5242_5c00381a-8c02-c491-e063-6394a90af78f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BELLIS PERENNIS
- Dosage form
- GLOBULE
- Route
- ORAL
- Labeler
- Total Operations Management LLC DBA:Bestmade Natural Products Micro
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2026-06-01
- Substance
- BELLIS PERENNIS WHOLE
- Active strength
- 30 [hp_C]/g
- 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
- BMNP BELLIS PERENNIS
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BELLIS PERENNIS WHOLE | 30 [hp_C]/g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82969-5242-1 | 82969524201 | 25 g in 1 BOTTLE, GLASS (82969-5242-1) | 25 g | 2026-06-01 | No | No | Current |
| 82969-5242-2 | 82969524202 | 8 g in 1 BOTTLE, GLASS (82969-5242-2) | 8 g | 2026-06-01 | No | No | Current |