FDA.reportPublic FDA data

DRUG FACTS:

Manufacturer
The Magni Company | Apotheca Company
Effective date
2026-05-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:38:30

Label at a glance#

ProductMigraine Relief
Active ingredientATROPA BELLADONNA, BRYONIA ALBA ROOT, MATRICARIA CHAMOMILLA WHOLE, BLACK COHOSH, ARABICA COFFEE BEAN, NITROGLYCERIN, IRIS VERSICOLOR ROOT, SODIUM CHLORIDE, PASSIFLORA INCARNATA FLOWERING TOP, VALERIAN
Label structure9 sections

Indications and uses

Temporarily relieves acute symptoms of migraine headaches such as: •pressure •pulsating •stabbing headache •nausea •sensitivity

Dosage and administration

Adults and children 12 years and above: Dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician. Children under 12 years: consult a physician Take at least 10 minutes before or after eating or drinking.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Belladonna 6X, 12X, Bryonia (Alba) 6X, 12X, 18X, Chamomilla 3X, Cimicifuga Racemosa 6X, 12X, 18X, Coffea Cruda 3X, Glonoinum 12X, 18X, Iris Versicolor 6X, 12X, 18X, Natrum Muriaticum 6X, 12X, 18X, Passiflora Incarnata 3X, Valeriana Officinalis 3X

USES:

OTC - PURPOSE SECTION

Temporarily relieves acute symptoms of migraine headaches such as:

•pressure

•pulsating

•stabbing headache

•nausea

•sensitivity

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Use only after diagnosis by a physician. This product is intended to complement, not replace,  proper medical attention.

Stop use and ask a doctor if you experience worsening symptoms or if symptoms last longer than 7 days.

Other Information

Store tightly closed in dry place.

Tamper Sealed: Sealed for your protection. Do not use if seal is broken or missing.

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic

Pharmacopeia of the United States.

These statements are supported by the traditional homeopathic principles.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and above:

Dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician.

Children under 12 years: consult a physician

Take at least 10 minutes before or after eating or drinking.

USES:

INDICATIONS & USAGE SECTION

Temporarily relieves acute symptoms of migraine headaches such as:

•pressure

•pulsating

•stabbing headache

•nausea

•sensitivity

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate, Microcrystaline Cellulose.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by: The Magni Group, Inc.  McKinney, TX 75074 USA

www.magnilife.com                               1-800-645-9199

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAGNILIFE Homeopathic
NDC 43689-0017-1
MIGRAINE RELIEF

Relieves Symptoms
of Migraine Headaches

√ Headache
√ Light Sensitivity
√ Noise Sensitivity
√ Blurred Vision
√ Nausea

90 Tablets
Dissolving Tablets

Migraine Relief LBLMigraine Relief LBL

Migraine Relief CTNMigraine Relief CTN

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
00358076-c817-430b-b924-11d717dc307cProduct name120160718
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43689-0017-22024-11-05C16284748780-1ba0f9c33-3cf6-a910-e053-dadaa90a0b85DRUG FACTS:
43689-0017-22024-01-30C16284748780-1ba0f9c33-3cf6-a910-e053-dadaa90a0b85DRUG FACTS:
43689-0017-22022-01-10C16284748780-1ba0f9c33-3cf6-a910-e053-dadaa90a0b85DRUG FACTS:
43689-0017-22021-01-29C16284748780-1ba0f9c33-3cf6-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43689-0017-1Migraine Relief90 in 1 BOTTLETABLET905
43689-0017-2Migraine Relief1 in 1 CARTONTABLET15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARABICA COFFEE BEANACTIVE INGREDIENT3SW678MX721
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H1
BLACK COHOSHACTIVE INGREDIENTK73E24S6X91
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B1
IRIS VERSICOLOR ROOTACTIVE INGREDIENTX43D4L3DQC1
MATRICARIA RECUTITAACTIVE INGREDIENTG0R4UBI2ZZ1
NITROGLYCERINACTIVE INGREDIENTG59M7S0WS31
PASSIFLORA INCARNATA FLOWERING TOPACTIVE INGREDIENTCLF5YFS11O1
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
VALERIANACTIVE INGREDIENTJWF5YAW3QW1
ARABICA COFFEE BEANACTIVE MOIETY3SW678MX721
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H1
BLACK COHOSHACTIVE MOIETYK73E24S6X91
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B1
CHLORIDE IONACTIVE MOIETYQ32ZN486981
IRIS VERSICOLOR ROOTACTIVE MOIETYX43D4L3DQC1
MATRICARIA RECUTITAACTIVE MOIETYG0R4UBI2ZZ1
NITROGLYCERINACTIVE MOIETYG59M7S0WS31
PASSIFLORA INCARNATA FLOWERING TOPACTIVE MOIETYCLF5YFS11O1
VALERIANACTIVE MOIETYJWF5YAW3QW1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I301

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43689-001743689-0017-1, 43689-0017-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ATROPA BELLADONNAWQZ3G9PF0HACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
MATRICARIA CHAMOMILLA WHOLEG0R4UBI2ZZACTIB
BLACK COHOSHK73E24S6X9ACTIB
ARABICA COFFEE BEAN3SW678MX72ACTIB
NITROGLYCERING59M7S0WS3ACTIB
IRIS VERSICOLOR ROOTX43D4L3DQCACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
PASSIFLORA INCARNATA FLOWERING TOPCLF5YFS11OACTIB
VALERIANJWF5YAW3QWACTIB
LACTOSEJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Migraine ReliefBELLADONNA, BRYONIA (ALBA), CHAMOMILLA, CIMICIFUGA RACEMOSA, COFFEA CRUDA, GLONOINUM, IRIS VERSICOLOR, NATRUM MURIATICUM, PASSIFLORA INCARNATA, VALERIANA OFFICINALISThe Magni Company79b25c52-e145-4ee5-af2e-1ccf6ad5ac2d2026-05-07WarningsExact identifier
ndc (package): 43689-0017-1
ndc (package): 43689-0017-2
ndc (product): 43689-0017
ndc11 (package): 43689001702
ndc11 (package): 43689001701
spl id: 39e553c6-af2a-43fa-a81d-04933b4dea91
spl set id: 79b25c52-e145-4ee5-af2e-1ccf6ad5ac2d

Reported adverse events (FAERS/openFDA)#

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