Bryophyllum Argentum Special Order
- Product NDC
- 48951-2166
- 11-digit product format
- 489512166
- Labeler code
- 48951
- Product ID
- 48951-2166_5ce1e7ab-7667-a126-e063-6294a90a2ee1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bryophyllum Argentum Special Order
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- SILVER; KALANCHOE DAIGREMONTIANA LEAF
- Active strength
- 6; 3 [hp_X]/mL; [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
- Bryophyllum Argentum Special Order
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SILVER | 6 [hp_X]/mL |
| KALANCHOE DAIGREMONTIANA LEAF | 3 [hp_X]/mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-2166-3 | 48951216603 | 60 mL in 1 BOTTLE, DROPPER (48951-2166-3) | 60 ml | 2009-09-01 | No | No | Current |