Occuloplex G

Product NDC
43857-0461
Requested package NDC
43857-0461-1
11-digit product format
438570461
Labeler code
43857
Product ID
43857-0461_8e78973a-78fd-45e1-87b0-872a391e2c43
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Euphrasia Officinalis, Ginkgo Biloba, Petroselinum Sativum, Vaccinium Myrtillus, Ascorbic Acid, Spigelia Anthelmia, Eye (Suis), Germanium Sesquioxide, Lithium Metallicum, Ubidecarenonum, Aurum Metallicum, Bryonia (Alba), Hepar Sulphuris Calcareum, Phosphorus, Ruta Graveolens, Sulphur
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-09-06
Marketing end
2022-10-16
Substance
EUPHRASIA STRICTA; GINKGO; PETROSELINUM CRISPUM; BILBERRY; ASCORBIC ACID; SPIGELIA ANTHELMIA; SUS SCROFA EYE; GERMANIUM SESQUIOXIDE; LITHIUM; UBIDECARENONE; GOLD; BRYONIA ALBA ROOT; CALCIUM SULFIDE; PHOSPHORUS; RUTA GRAVEOLENS FLOWERING TOP; SULFUR
Active strength
3 [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
Pharmacologic classes
Vitamin C [EPC],Ascorbic Acid [CS],Mood Stabilizer [EPC],Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Allergens [CS],Cell-mediated Immunity [PE]
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 packagepackage43857-046143857-0461-1DDiscontinued by firm2026-08-17

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
43857-0461-14385704610130 mL in 1 BOTTLE, DROPPER (43857-0461-1) 30 ml2017-09-062022-10-16NoNoCurrent