ASP
- Product NDC
- 43857-0291
- 11-digit product format
- 438570291
- Labeler code
- 43857
- Product ID
- 43857-0291_7bd3a4ed-6366-4c9e-9c13-2bd602f5f251
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Hydrastis canadensis, Tabebuia impetiginosa, Glandula suprarenalis suis, Thymus(suis), Thyroidinum (suis), Arsenicum album,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-04-03
- Marketing end
- 0000-00-00
- Substance
- ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; TABEBUIA IMPETIGINOSA BARK; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; SUS SCROFA THYROID; ARSENIC TRIOXIDE; BRYONIA ALBA ROOT; ANAMIRTA COCCULUS SEED; COLCHICUM AUTUMNALE BULB; LEDUM PALUSTRE TWIG; MERCURIC CYANIDE; SODIUM SULFATE; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; ASPERGILLUS FLAVUS
- 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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#