Bio Placenta Phase

Product NDC

43742-0855

11-digit product format

437420855

Labeler code

43742

Product ID

43742-0855_b1e1c518-d2c7-4343-a47e-fa8a04b64ec1

Type

HUMAN OTC DRUG

Nonproprietary name

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

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2016-09-19

Marketing end

2023-01-22

Substance

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

Active strength

4 [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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record