Home NDC 44911-0378-1 Septastat
Product NDC 44911-0378
Requested package NDC 44911-0378-1
11-digit product format 449110378
Labeler code 44911
Product ID 44911-0378_f193c9d5-2942-4d93-9ffe-158b01687d80
Type HUMAN OTC DRUG
Nonproprietary name Baptisia Tinctoria, Echinacea (Angustifolia), Anthracinum, Arsenicum Album, Belladonna, Crotalus Horridus, Hyoscyamus Niger, Lachesis Mutus, Pyrogenium, Tarentula Cubensis
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-07-27
Marketing end 2024-03-19
Substance BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; ARSENIC TRIOXIDE; ATROPA BELLADONNA; CROTALUS HORRIDUS HORRIDUS VENOM; HYOSCYAMUS NIGER; LACHESIS MUTA VENOM; RANCID BEEF; CITHARACANTHUS SPINICRUS
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; 1/mL
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 44911-0378-1 44911037801 30 mL in 1 BOTTLE, DROPPER (44911-0378-1) 30 ml 2016-07-27 2024-03-19 No No Current