Argentite Urtica Special Order
- Product NDC
- 48951-1220
- 11-digit product format
- 489511220
- Labeler code
- 48951
- Product ID
- 48951-1220_553f34f1-83f8-67b1-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Argentite Urtica Special Order
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SAW PALMETTO; URTICA DIOICA; ROYAL JELLY; SILVER SULFIDE; BOS TAURUS PITUITARY GLAND; BOS TAURUS TESTICLE
- Active strength
- 4 [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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 48951-1220 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 48951-1220 | 48951-1220-1 | D | Discontinued by firm | 2026-07-31 |