Helleborus comp. A
- Product NDC
- 48951-5122
- 11-digit product format
- 489515122
- Labeler code
- 48951
- Product ID
- 48951-5122_bd490a1c-9c75-4585-e053-2995a90a4785
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Helleborus comp. A
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2021-03-11
- Marketing end
- 0000-00-00
- Substance
- PHOSPHORUS; ARSENIC TRIOXIDE; LEAD MONOSILICATE; SILVER; FORMICA RUFA; ANTIMONY; HELLEBORUS NIGER ROOT
- Active strength
- 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-5122-1 | 48951512201 | 10 AMPULE in 1 BOX (48951-5122-1) > 1 mL in 1 AMPULE | 10 ampule | 2021-03-11 | 0000-00-00 | No | No | Current |