HGH Vitality

Product NDC
43742-1299
Requested package NDC
43742-1299-1
11-digit product format
437421299
Labeler code
43742
Product ID
43742-1299_bd2c1674-96dd-48f9-b2ba-e2054169406c
Type
HUMAN OTC DRUG
Nonproprietary name
Agnus Castus, Ambra Grisea, Apiolum, Estradiol, Estriol, L-Dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, alpha-Lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Conium Maculatum, Selenium Metallicum, Folliculinum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (Suis), Lymph Node (Suis), Medulla Ossis Suis, Oophorinum (Suis), Orchitinum (Suis), Pancreas Suis, Spleen (Suis), Human Growth Hormone, Proteus
Dosage form
TABLET
Route
ORAL
Labeler
Deseret Biologicals
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-03-14
Marketing end
2024-04-16
Substance
CHASTE TREE; AMBERGRIS; APIOLE (PARSLEY); ESTRADIOL; ESTRIOL; LEVODOPA; MELATONIN; TESTOSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; .ALPHA.-LIPOIC ACID; NADIDE; PANTOTHENIC ACID; LACTIC ACID, L-; UBIDECARENONE; BARIUM CARBONATE; CONIUM MACULATUM FLOWERING TOP; SELENIUM; ESTRONE; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA BONE MARROW; SUS SCROFA OVARY; SUS SCROFA TESTICLE; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; SOMATROPIN; PROTEUS MORGANII
Active strength
6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_C]/1
DEA schedule
CIII
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 packagepackage43742-129943742-1299-1DDiscontinued by firm2026-10-05

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…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1299-14374212990190 TABLET in 1 BOTTLE (43742-1299-1) 90 tablet2019-03-142024-04-16NoNoCurrent