Bio Placenta Phase

Product NDC

43742-2240

11-digit product format

437422240

Labeler code

43742

Product ID

43742-2240_e5d80302-57fa-4048-a119-0a325139f8d6

Type

HUMAN OTC DRUG

Nonproprietary name

Aesculus Hippocastanum, Arteria Suis, Astragalus Exscapus, Baryta Carbonica, Cuprum Sulphuricum, DHEA (Dehydroepiandrosterone), Funiculus Umbilicalis Suis, Melilotus Officinalis, Natrum Pyruvicum, Placenta Totalis Suis, Plumbum Iodatum, Proteus (Vulgaris), Quercetin, Rutin, Sarcolacticum Acidum, Secale Cornutum, Solanum Nigrum, Strophanthus Hispidus, Tabacum, Vena Suis, Vipera Berus

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2024-11-19

Substance

ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING; BARIUM CARBONATE; CLAVICEPS PURPUREA SCLEROTIUM; CUPRIC SULFATE; HORSE CHESTNUT; LACTIC ACID, L-; LEAD IODIDE; MELILOTUS OFFICINALIS TOP; PRASTERONE; PROTEUS VULGARIS; QUERCETIN; RUTIN; SODIUM PYRUVATE; SOLANUM NIGRUM WHOLE; STROPHANTHUS HISPIDUS SEED; SUS SCROFA ARTERY; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; SUS SCROFA VEIN; TOBACCO LEAF; VIPERA BERUS VENOM

Active strength

6; 13; 8; 6; 4; 4; 18; 6; 6; 30; 6; 6; 8; 6; 6; 10; 6; 10; 8; 10; 20 [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_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

Pharmacologic classes

Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes