ASP

Product NDC

43857-0426

11-digit product format

438570426

Labeler code

43857

Product ID

43857-0426_b771f9ee-6d61-40ae-a224-4a5b47bfd668

Type

HUMAN OTC DRUG

Nonproprietary name

Echinacea (Angustifolia), Tabebuia Impetiginosa, Hydrastis Canadensis, Glandula Suprarenalis Suis, Thymus (Suis), Thyroidinum (Suis), Arsenicum Album, Bryonia (Alba), Cocculus Indicus, Colchicum Autumnale, Ledum Palustre, Mercurius Cyanatus, Natrum Sulphuricum, Pulsatilla (Vulgaris) Sepia, Silicea, Aspergillus Flavus

Dosage form

LIQUID

Route

ORAL

Labeler

BioActive Nutritional, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2017-01-24

Marketing end

2024-02-18

Substance

ECHINACEA ANGUSTIFOLIA; HANDROANTHUS IMPETIGINOSUS BARK; GOLDENSEAL; 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

0000-00-00

Current FDA listing

Historical FDA.report record