Home NDC 44911-0537-1 BAC
Product NDC 44911-0537
Requested package NDC 44911-0537-1
11-digit product format 449110537
Labeler code 44911
Product ID 44911-0537_020e3001-6ad2-40b4-9307-0564d2822542
Type HUMAN OTC DRUG
Nonproprietary name Apis Mellifica, Arsenicum Album, Belladonna, Chamomilla, Echinacea (Angustifolia), Lachesis Mutus, Mercurius Solubilis, Pulsatilla (Pratensis), Pyrogenium, Rhus Tox, Silicea
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-03-27
Marketing end 2025-04-14
Substance ANEMONE PRATENSIS; APIS MELLIFERA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; ECHINACEA ANGUSTIFOLIA WHOLE; LACHESIS MUTA VENOM; MATRICARIA CHAMOMILLA WHOLE; MERCURIUS SOLUBILIS; RANCID BEEF; SILICON DIOXIDE; 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; [hp_X]/mL
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
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 · 4 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…2022-04-09 23:13 UTC · source 2022-04-08 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 I Inactivated by FDA bd6a592717d7…303034d00443…
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 44911-0537-1 44911053701 30 mL in 1 BOTTLE, DROPPER (44911-0537-1) 30 ml 2020-03-27 2025-04-14 No No Current