VAX

Product NDC

43857-0453

11-digit product format

438570453

Labeler code

43857

Product ID

43857-0453_1322732d-5d86-4b79-bd55-91aebccb013d

Type

HUMAN OTC DRUG

Nonproprietary name

Baptisia Tinctoria, Echinacea (Angustifolia), 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, Hydrastis Canadensis, 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

2017-07-20

Substance

ANTIMONY TRISULFIDE; ARNICA MONTANA; ARSENIC TRIOXIDE; ASTRAGALUS PROPINQUUS ROOT; ATROPA BELLADONNA; BAPTISIA TINCTORIA; BORDETELLA PERTUSSIS; CALENDULA OFFICINALIS FLOWERING TOP; CHAMOMILE; CHELIDONIUM MAJUS; ECHINACEA ANGUSTIFOLIA; FENUGREEK SEED; GOLDENSEAL; LIGUSTICUM PORTERI ROOT; LOMATIUM DISSECTUM ROOT; LYCOPODIUM CLAVATUM SPORE; MYRRH; NASTURTIUM OFFICINALE; PHYTOLACCA AMERICANA ROOT; PROPOLIS WAX; SILICON DIOXIDE; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; TABEBUIA IMPETIGINOSA BARK; TARAXACUM OFFICINALE; TETANUS TOXIN; THIMEROSAL; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF; TRIFOLIUM PRATENSE FLOWER; URTICA DIOICA; VERONICASTRUM VIRGINICUM ROOT

Active strength

30; 4; 12; 6; 12; 3; 30; 4; 12; 4; 3; 4; 5; 4; 4; 12; 4; 4; 4; 6; 30; 8; 8; 3; 4; 30; 30; 30; 12; 3; 4; 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes