Bryophyllum Argentum
- Product NDC
- 48951-2165
- 11-digit product format
- 489512165
- Labeler code
- 48951
- Product ID
- 48951-2165_5ce1ad6a-afad-e05f-e063-6394a90a7a19
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bryophyllum Argentum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- KALANCHOE DAIGREMONTIANA LEAF; SILVER
- Active strength
- 3; 6 [hp_X]/1; [hp_X]/1
- 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
- Bryophyllum Argentum
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| KALANCHOE DAIGREMONTIANA LEAF | 3 [hp_X]/1 |
| SILVER | 6 [hp_X]/1 |
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-2165-2 | 48951216502 | 1350 PELLET in 1 BOTTLE, GLASS (48951-2165-2) | 1350 pellet | 2009-09-01 | No | No | Current |