Ver

Product NDC
43742-1032
Requested package NDC
43742-1032-1
11-digit product format
437421032
Labeler code
43742
Product ID
43742-1032_67cb2a5b-9df9-4b22-9c4f-1f1536b79bf7
Type
HUMAN OTC DRUG
Nonproprietary name
Filix Mas, Artemisia Vulgaris, Cina, Melilotus Officinalis, Quassia (Amara), Spigelia Anthelmia, Teucrium Marum, Thymus Serpyllum, Silicea, Calcarea Carbonica, Graphites, Iodium, Mercurius Corrosivus, Sabadilla, Ascaris Lumbricoides, Trichinella Spiralis, Enterobius Vermicularis, Taenia Solium, Trichomonas Vaginalis, Giardia Lamblia, Cryptosporidium Parvum, Taenia Saginata, Brugia Malayi
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-06-22
Marketing end
2022-12-02
Substance
DRYOPTERIS FILIX-MAS ROOT; ARTEMISIA VULGARIS ROOT; ARTEMISIA CINA PRE-FLOWERING TOP; MELILOTUS OFFICINALIS TOP; QUASSIA AMARA WOOD; TEUCRIUM MARUM; THYMUS SERPYLLUM; SPIGELIA ANTHELMIA; SILICON DIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; GRAPHITE; IODINE; MERCURIC CHLORIDE; SCHOENOCAULON OFFICINALE SEED; ASCARIS LUMBRICOIDES; TRICHINELLA SPIRALIS; ENTEROBIUS VERMICULARIS; TAENIA SOLIUM; TRICHOMONAS VAGINALIS; GIARDIA LAMBLIA; CRYPTOSPORIDIUM PARVUM; TAENIA SAGINATA; BRUGIA MALAYI
Active strength
1 [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; [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 packagepackage43742-103243742-1032-1DDiscontinued 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
43742-1032-14374210320160 mL in 1 BOTTLE, DROPPER (43742-1032-1) 60 ml2017-06-222022-12-02NoNoCurrent