FNG

Product NDC

43742-1575

11-digit product format

437421575

Labeler code

43742

Product ID

43742-1575_1c3d5284-5fa2-4fa0-bab7-d522ff61b56e

Type

HUMAN OTC DRUG

Nonproprietary name

Berberis Vulgaris, Cochlearia Armoracia, Echinacea (Angustifolia), Lomatium Dissectum, Myrrha, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Tabebuia Impetiginosa, Thymus (Suis), Formalinum, Carbolicum Acidum, Ferrum Metallicum, Iridium Metallicum, Lycopodium Clavatum, Phosphoricum Acidum, Pulsatilla (Prastensis), Selenium Metallicum, Zincum Metallicum, Adenosinum Triphosphoricum Dinatrum, Alternaria Tenuis Nees, Aspergillus Niger, Candida Albicans, Candida Parapsilosis, Torula Cerevisiae,

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2019-10-01

Marketing end

2024-10-01

Substance

BERBERIS VULGARIS ROOT BARK; HORSERADISH; ECHINACEA ANGUSTIFOLIA; LOMATIUM DISSECTUM ROOT; MYRRH; GOLDENSEAL; PROPOLIS WAX; SUS SCROFA ADRENAL GLAND; TABEBUIA IMPETIGINOSA BARK; SUS SCROFA THYMUS; FORMALDEHYDE; PHENOL; IRON; IRIDIUM; LYCOPODIUM CLAVATUM SPORE; PHOSPHORIC ACID; ANEMONE PRATENSIS; SELENIUM; ZINC; ADENOSINE TRIPHOSPHATE DISODIUM; ALTERNARIA ALTERNATA; ASPERGILLUS NIGER VAR. NIGER; CANDIDA ALBICANS; CANDIDA PARAPSILOSIS; SACCHAROMYCES CEREVISIAE; METHYLCOBALAMIN; LACTIC ACID, L-; MUCOR RACEMOSUS; RHIZOPUS STOLONIFER; ESCHERICHIA COLI; BRUGIA MALAYI

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_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record