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 80 of 109 · 2,172 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VALERIANA OFFICINALISVALERIANBoiron85f2d7b5-0658-2f07-e053-2a91aa0ad6562023-11-15Exact identifier
unii: JWF5YAW3QW
Natrum muriaticumSODIUM CHLORIDEBoiron8646d7ea-cf5e-607d-e053-2a91aa0aeca12023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron86466121-7217-d053-e053-2a91aa0a8f8a2023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron864669c9-5bdc-232f-e053-2a91aa0a1fc62023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron86462e06-d221-36b7-e053-2991aa0a1d822023-11-14Exact identifier
unii: 451W47IQ8X
GlonoinumNITROGLYCERINBoiron85a1163a-fe45-e31a-e053-2991aa0a64662023-11-13Exact identifier
unii: G59M7S0WS3
GlonoinumNITROGLYCERINBoiron85a39d5c-2b11-62ed-e053-2a91aa0a0a312023-11-13Exact identifier
unii: G59M7S0WS3
GlonoinumNITROGLYCERINBoiron85a33a5a-41c6-3d84-e053-2a91aa0a6ec72023-11-13Exact identifier
unii: G59M7S0WS3
GlonoinumNITROGLYCERINBoiron7c0efc90-7a53-11e6-a302-424c583030312023-11-13Exact identifier
unii: G59M7S0WS3
Iris versicolorIRIS VERSICOLOR ROOTBoiron85cec3a4-c752-bcaf-e053-2a91aa0a7ef62023-11-13Exact identifier
unii: X43D4L3DQC
Iris versicolorIRIS VERSICOLOR ROOTBoiron85cea89c-b156-57b8-e053-2a91aa0af7152023-11-13Exact identifier
unii: X43D4L3DQC
Iris versicolorIRIS VERSICOLOR ROOTBoiron36917aa0-2a55-11e7-831a-424c583030312023-11-13Exact identifier
unii: X43D4L3DQC
BelladonnaATROPA BELLADONNABoiron850051dc-356f-33c5-e053-2a91aa0ae67d2023-11-09Exact identifier
unii: WQZ3G9PF0H
BelladonnaATROPA BELLADONNABoiron84767820-0e29-3f25-e053-2a91aa0a6a182023-11-09Exact identifier
unii: WQZ3G9PF0H
BelladonnaATROPA BELLADONNABoironb0b40260-79fe-11e6-9491-424c583030312023-11-09Exact identifier
unii: WQZ3G9PF0H
Cimifuga racemosaBLACK COHOSHBoiron852a6651-24bf-2c72-e053-2a91aa0a838b2023-11-09Exact identifier
unii: K73E24S6X9
Cimifuga racemosaBLACK COHOSHBoiron852a47e0-e9de-ae5e-e053-2991aa0a030b2023-11-09Exact identifier
unii: K73E24S6X9
Cimifuga racemosaBLACK COHOSHBoiron852a3251-bf29-5557-e053-2991aa0a4fbd2023-11-09Exact identifier
unii: K73E24S6X9
Cimifuga racemosaBLACK COHOSHBoiron852acb2d-8cf8-1c86-e053-2a91aa0a13e92023-11-09Exact identifier
unii: K73E24S6X9
Cimifuga racemosaBLACK COHOSHBoiron8529e7f1-0c8e-ab5d-e053-2991aa0ab4122023-11-09Exact identifier
unii: K73E24S6X9

Reported adverse events (FAERS/openFDA)#

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