Home NDC 44911-0523-1 Organdrainex
Product NDC 44911-0523
Requested package NDC 44911-0523-1
11-digit product format 449110523
Labeler code 44911
Product ID 44911-0523_6eed96f6-639a-4325-9eae-f735d6241043
Type HUMAN OTC DRUG
Nonproprietary name Allium Cepa, Allium Sativum, Ambrosia Artemisiaefolia, Berberis Vulgaris, Chelidonium Majus, Collinsonia Canadensis, Cynara Scolymus, Petroselinum Sativum, Trifolium Pratense, Methylcobalamin, Aloe, Alpha-Lipoicum Acidum, Palladium Metallicum
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-01-29
Marketing end 2025-03-03
Substance ALOE; ALPHA LIPOIC ACID; AMBROSIA ARTEMISIIFOLIA WHOLE; BERBERIS VULGARIS ROOT BARK; CHELIDONIUM MAJUS WHOLE; COLLINSONIA CANADENSIS ROOT; CYNARA SCOLYMUS LEAF; GARLIC; METHYLCOBALAMIN; ONION; PALLADIUM; PETROSELINUM CRISPUM WHOLE; TRIFOLIUM PRATENSE FLOWER
Active strength 6 [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; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [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…2022-08-30 03:57 UTC · source 2022-08-29 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…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 44911-0523-1 44911052301 118 mL in 1 BOTTLE, GLASS (44911-0523-1) 118 ml 2020-01-29 2025-03-03 No No Current