Home NDC 44911-0443-1 Vaccistat
Product NDC 44911-0443
Requested package NDC 44911-0443-1
11-digit product format 449110443
Labeler code 44911
Product ID 44911-0443_58818186-7b29-40e4-9548-5d89dc0fd305
Type HUMAN OTC DRUG
Nonproprietary name Baptisia Tinctoria, Echinacea (Angustifolia), Hydrastis Canadensis, Antimonium Tartaricum, Mezereum, Mercurius Solubilis, Silicea, Thuja Occidentalis, Malandrinum, Variolinum
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-09-28
Marketing end 2025-01-20
Substance ANTIMONY POTASSIUM TARTRATE; BAPTISIA TINCTORIA ROOT; DAPHNE MEZEREUM BARK; ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; MERCURIUS SOLUBILIS; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAFY TWIG; VACCINIA VIRUS; VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN
Active strength 12 [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
Pharmacologic classes Actively Acquired Immunity [PE], Live Vaccinia Virus Vaccine [EPC], Smallpox Vaccine [CS], Vaccines, Live, Unattenuated [CS]
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record 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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 D Discontinued by firm ed331223b511…672a5bd82f5f…2021-12-27 23:28 UTC · source 2021-12-27 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0443-1 44911044301 30 mL in 1 BOTTLE, DROPPER (44911-0443-1) 30 ml 2017-09-28 2025-01-20 No No Current