VAX
- Product NDC
- 43857-0386
- 11-digit product format
- 438570386
- Labeler code
- 43857
- Product ID
- 43857-0386_a677a213-3902-4589-a5f7-8b603bcc776e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Baptisia Tinctoria, Echinacea (Angustifolia), Hydrastis Canadensis, Tabebuia Impetiginosa, Trifolium Pratense, Arnica Montana, Calendula Officinalis, Chelidonium Majus, Leptandra Virginica, Ligusticum Porteri, Lomatium Dissectum, Myrrha, Nasturtium Aquaticum, Phytolacca Decandra, Taraxacum Officinale, Trigonella Foenum-Graecum, Urtica Dioica, Astragalus Membranaceus, Propolis, Glandula Suprarenalis Suis, Thymus (Suis), Arsenicum Album, Belladonna, Chamomilla, Lycopodium Clavatum, Rhus Tox, Silicea,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-01-21
- Marketing end
- 0000-00-00
- Substance
- BAPTISIA TINCTORIA; ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; TABEBUIA IMPETIGINOSA BARK; TRIFOLIUM PRATENSE FLOWER; ARNICA MONTANA; CALENDULA OFFICINALIS FLOWERING TOP; CHELIDONIUM MAJUS; VERONICASTRUM VIRGINICUM ROOT; LIGUSTICUM PORTERI ROOT; LOMATIUM DISSECTUM ROOT; MYRRH; NASTURTIUM AQUATICUM; PHYTOLACCA AMERICANA ROOT; TARAXACUM OFFICINALE; FENUGREEK SEED; URTICA DIOICA; ASTRAGALUS PROPINQUUS ROOT; PROPOLIS WAX; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; ARSENIC TRIOXIDE; ATROPA BELLADONNA; CHAMOMILE; LYCOPODIUM CLAVATUM SPORE; TOXICODENDRON PUBESCENS LEAF; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAFY TWIG; ANTIMONY TRISULFIDE; BORDETELLA PERTUSSIS; TETANUS TOXIN; THIMEROSAL
- 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; [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_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#