Headache
- Product NDC
- 43857-0050
- 11-digit product format
- 438570050
- Labeler code
- 43857
- Product ID
- 43857-0050_b5b81025-8777-4f58-bc2e-9b87f3a6a34f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Melilotus officinalis, Spigelia anthelmia, Allium cepa, Belladonna, Bryonia, Cimicifuga racemosa, Gelsemium Sempervirens, Glonoinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-07-18
- Marketing end
- 2020-04-21
- Substance
- MELILOTUS OFFICINALIS TOP; SPIGELIA ANTHELMIA; ONION; ATROPA BELLADONNA ROOT; BRYONIA ALBA ROOT; BLACK COHOSH; GELSEMIUM SEMPERVIRENS ROOT; NITROGLYCERIN; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; STRYCHNOS NUX-VOMICA SEED; SANGUINARIA CANADENSIS WHOLE; SILICON DIOXIDE; CITHARACANTHUS SPINICRUS
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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
- 0000-00-00
- 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 | 43857-0050 | D | Discontinued by firm | 2026-08-03 | ||
| excluded package | package | 43857-0050 | 43857-0050-1 | D | Discontinued by firm | 2026-08-03 |