EBV Stat

Product NDC
44911-0524
Requested package NDC
44911-0524-1
11-digit product format
449110524
Labeler code
44911
Product ID
44911-0524_77fb698b-cb0b-4930-9942-5486a28555f5
Type
HUMAN OTC DRUG
Nonproprietary name
Astragalus Membranaceus, Echinacea (Angustifolia), Phytolacca Decandra, Hydrastis Canadensis, Aranea Diadema, Iridium Metallicum, Lycopodium Clavatum, Rhus Tox, Silicea, Sepia, Epstein-Barr Virus Nosode
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-02-24
Marketing end
2025-02-17
Substance
ARANEUS DIADEMATUS; ASTRAGALUS PROPINQUUS ROOT; ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; HUMAN HERPESVIRUS 4; IRIDIUM; LYCOPODIUM CLAVATUM SPORE; PHYTOLACCA AMERICANA ROOT; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; TOXICODENDRON PUBESCENS LEAF
Active strength
12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/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 packagepackage44911-052444911-0524-1DDiscontinued by firm2026-10-15

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 · 6 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…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0524-12022-03-23C16284748780-1d6a99b39-3347-a426-e053-dadaa90af4c2Drug Facts:
44911-0524-12022-01-28C16284748780-1d6a99b39-3347-a426-e053-dadaa90af4c2Drug Facts:

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0524-14491105240130 mL in 1 BOTTLE, DROPPER (44911-0524-1) 30 ml2020-02-242025-02-17NoNoCurrent