Bio Placenta Phase

Product NDC
43742-2240
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
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
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
43742-2240-130 mL in 1 BOTTLE, DROPPER (43742-2240-1) 2024-11-19NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
DRUG FACTS:Deseret Biologicals, Inc. | Apotheca Company2024-11-18HUMAN OTC DRUG LABEL1