Bio Placenta Phase

Product NDC
43742-0855
Requested package NDC
43742-0855-1
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage43742-085543742-0855-1DDiscontinued by firm2026-08-11

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-0855-14374208550130 mL in 1 PACKAGE (43742-0855-1) 30 ml2016-09-192023-01-22NoNoCurrent