Home NDC 43689-0010-2 Migraine Relief
Product NDC 43689-0010
Requested package NDC 43689-0010-2
11-digit product format 436890010
Labeler code 43689
Product ID 43689-0010_f2faa306-5edf-464e-93ae-ccc255ab182b
Type HUMAN OTC DRUG
Nonproprietary name not applicable
Dosage form TABLET, ORALLY DISINTEGRATING
Route ORAL
Labeler The Magni Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2014-07-17
Marketing end 2023-01-26
Substance ARABICA COFFEE BEAN; ATROPA BELLADONNA; BLACK COHOSH; BRYONIA ALBA ROOT; IRIS VERSICOLOR ROOT; MATRICARIA RECUTITA; NITROGLYCERIN; PASSIFLORA INCARNATA FLOWERING TOP; SODIUM CHLORIDE; VALERIAN
Active strength 3 [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vasodilation [PE]
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 · 15 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…2024-07-10 04:00 UTC · source 2024-07-09 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2021-12-27 23:28 UTC · source 2021-12-27 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ARABICA COFFEE BEAN ACTIVE INGREDIENT 3SW678MX72 MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 ATROPA BELLADONNA ACTIVE INGREDIENT WQZ3G9PF0H MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 BLACK COHOSH ACTIVE INGREDIENT K73E24S6X9 MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 BRYONIA ALBA ROOT ACTIVE INGREDIENT T7J046YI2B MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 IRIS VERSICOLOR ROOT ACTIVE INGREDIENT X43D4L3DQC MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 MATRICARIA RECUTITA ACTIVE INGREDIENT G0R4UBI2ZZ MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 NITROGLYCERIN ACTIVE INGREDIENT G59M7S0WS3 MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 PASSIFLORA INCARNATA FLOWERING TOP ACTIVE INGREDIENT CLF5YFS11O MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 VALERIAN ACTIVE INGREDIENT JWF5YAW3QW MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 ARABICA COFFEE BEAN ACTIVE MOIETY 3SW678MX72 MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 ATROPA BELLADONNA ACTIVE MOIETY WQZ3G9PF0H MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 BLACK COHOSH ACTIVE MOIETY K73E24S6X9 MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 BRYONIA ALBA ROOT ACTIVE MOIETY T7J046YI2B MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 CHLORIDE ION ACTIVE MOIETY Q32ZN48698 MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 IRIS VERSICOLOR ROOT ACTIVE MOIETY X43D4L3DQC MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 MATRICARIA RECUTITA ACTIVE MOIETY G0R4UBI2ZZ MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 NITROGLYCERIN ACTIVE MOIETY G59M7S0WS3 MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 PASSIFLORA INCARNATA FLOWERING TOP ACTIVE MOIETY CLF5YFS11O MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 VALERIAN ACTIVE MOIETY JWF5YAW3QW MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 LACTOSE INACTIVE INGREDIENT J2B2A4N98G MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY] 2
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43689-0010-2 43689001002 1 BOTTLE in 1 CARTON (43689-0010-2) > 10800 mg in 1 BOTTLE (43689-0010-1) 1 bottle 2014-07-17 2023-01-26 No No Current