Home NDC 44911-0364-1 HZ Neurapain
Product NDC 44911-0364
Requested package NDC 44911-0364-1
11-digit product format 449110364
Labeler code 44911
Product ID 44911-0364_e93c96c8-7875-42ae-9182-d554dae967ea
Type HUMAN OTC DRUG
Nonproprietary name Echinacea (Angustifolia), Kali Phosphoricum, Sarracenia Purpurea, Arsenicum Album, Causticum, Dolichos Pruriens, Hypericum Perforatum, Mezereum, Ranunculus Bulbosus, Rhus Tox
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-06-15
Marketing end 2024-07-23
Substance ARSENIC TRIOXIDE; CAUSTICUM; DAPHNE MEZEREUM BARK; ECHINACEA ANGUSTIFOLIA; HYPERICUM PERFORATUM; MUCUNA PRURIENS FRUIT TRICHOME; POTASSIUM PHOSPHATE, DIBASIC; RANUNCULUS BULBOSUS; SARRACENIA PURPUREA; TOXICODENDRON PUBESCENS LEAF
Active strength 30 [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
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, 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…2025-01-11 03:41 UTC · source 2025-01-10 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 D Discontinued by firm 367a005e9d99…383a685ebd0f…2021-12-27 23:28 UTC · source 2021-12-27 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…
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 44911-0364-1 44911036401 30 mL in 1 BOTTLE, DROPPER (44911-0364-1) 30 ml 2016-06-15 2024-07-23 No No Current