FDA.reportPublic FDA data

NDC 43689-0010-1 - Migraine Relief

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
43689-0010
Requested NDC
43689-0010-1
Package NDCs from labels
43689-0010-1, 43689-0010-2
Manufacturer
The Magni Company | Apotheca Company
Effective date
2022-02-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Migraine Relief - The Magni Company | Apotheca CompanyThe Magni Company | Apotheca Company2022-02-03HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43689-0010-22022-02-03C16284748780-19d75b9d0-72d6-f424-e053-dadaa90a57ceDRUG FACTS
43689-0010-22020-01-31C16284748780-19d75b9d0-72d6-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARABICA COFFEE BEANACTIVE INGREDIENT3SW678MX72MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0HMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
BLACK COHOSHACTIVE INGREDIENTK73E24S6X9MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2BMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
IRIS VERSICOLOR ROOTACTIVE INGREDIENTX43D4L3DQCMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
MATRICARIA RECUTITAACTIVE INGREDIENTG0R4UBI2ZZMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
NITROGLYCERINACTIVE INGREDIENTG59M7S0WS3MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
PASSIFLORA INCARNATA FLOWERING TOPACTIVE INGREDIENTCLF5YFS11OMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8XMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
VALERIANACTIVE INGREDIENTJWF5YAW3QWMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
ARABICA COFFEE BEANACTIVE MOIETY3SW678MX72MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0HMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
BLACK COHOSHACTIVE MOIETYK73E24S6X9MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2BMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
CHLORIDE IONACTIVE MOIETYQ32ZN48698MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
IRIS VERSICOLOR ROOTACTIVE MOIETYX43D4L3DQCMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
MATRICARIA RECUTITAACTIVE MOIETYG0R4UBI2ZZMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
NITROGLYCERINACTIVE MOIETYG59M7S0WS3MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
PASSIFLORA INCARNATA FLOWERING TOPACTIVE MOIETYCLF5YFS11OMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
VALERIANACTIVE MOIETYJWF5YAW3QWMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GMIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MIGRAINE RELIEF (NOT APPLICABLE) TABLET, ORALLY DISINTEGRATING [THE MAGNI COMPANY]2

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 35 of 113 · 2,257 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Coffea crudaARABICA COFFEE BEANBoiron853d2d9a-0c2c-22d0-e053-2a91aa0abaf82025-11-05Exact identifier
unii: 3SW678MX72
Coffea crudaARABICA COFFEE BEANBoiron853dc617-a8b6-7626-e053-2a91aa0a9ec72025-11-05Exact identifier
unii: 3SW678MX72
Coffea crudaARABICA COFFEE BEANBoiron853d570d-59ca-7e1f-e053-2a91aa0a5f1f2025-11-05Exact identifier
unii: 3SW678MX72
Coffea crudaARABICA COFFEE BEANBoiron853cb3dd-773a-208c-e053-2a91aa0a61892025-11-05Exact identifier
unii: 3SW678MX72
Coffea crudaARABICA COFFEE BEANBoiron755c0d20-7a53-11e6-ad11-424c583030312025-11-05Exact identifier
unii: 3SW678MX72
Coffea crudaARABICA COFFEE BEANBoiron853cdfcd-6a94-3462-e053-2a91aa0a750e2025-11-05Exact identifier
unii: 3SW678MX72
Dextrose in Lactated RingersDEXTROSE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.190da07e-a616-46e6-b4e5-1c0ba39306e52025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.f6d82772-638c-4584-b9d3-8833669f59632025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Com-Pare2 Dual Yeast Relief Plus Multi-symptom FormulaCANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, SULPHURTRP Company42b6b9b9-a673-0bba-e063-6394a90a88662025-11-03WarningsExact identifier
unii: 451W47IQ8X
Potassium Chloride in Dextrose and Sodium ChlorideDEXTROSE MONOHYDRATE, SODIUM CHLORIDE, AND POTASSIUM CHLORIDEICU Medical Inc.d8ee14e9-6733-4813-9f21-2b043a5f71882025-11-02Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Dextrose and Sodium ChlorideDEXTROSE MONOHYDRATE AND SODIUM CHLORIDEICU Medical Inc.4555b1bf-6d97-4798-a63d-6d34291c85ce2025-11-02Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Potassium Chloride in Sodium ChlorideSODIUM CHLORIDE AND POTASSIUM CHLORIDEICU Medical Inc.9dd1c001-73b3-41d4-9a96-61f6ad3a5dc32025-11-02Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDEICU Medical Inc.3cfdeee0-ff14-4341-8396-b11c2a037c602025-11-02Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDEICU Medical Inc.5f372b75-d7a4-471e-8ac6-290040fc84b02025-11-02Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Potassium Chloride in Sodium ChlorideSODIUM CHLORIDE AND POTASSIUM CHLORIDEICU Medical Inc.243fe8fc-996a-4855-8daf-069628e547c42025-11-02Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Lactated Ringers and DextroseSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATEICU Medical Inc.d310d170-5eeb-471b-af1a-0e845001d21d2025-11-02Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Family Care SalineSODIUM CHLORIDEUnited Exchange Corp.06737393-d4ae-3e7b-e063-6394a90ac19f2025-10-31WarningsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDEICU Medical Inc.009bef3c-e8ac-46be-b564-a2556adf00812025-10-31Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Potassium Chloride in Lactated Ringers and DextrosePOTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM LACTATE, AND DEXTROSE MONOHYDRATEICU Medical Inc.237b39fa-916e-4a54-99c8-4ae9ad54f0562025-10-30Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Avena ValerianaAVENA VALERIANAUriel Pharmacy Inc.54c206d5-c480-4214-813d-c009e1a26f1a2025-10-30WarningsExact identifier
unii: JWF5YAW3QW

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.