Migraine Headache Therapy

Product NDC
17312-041
11-digit product format
173120041
Labeler code
17312
Product ID
17312-041_4604cabb-ce20-ae65-e063-6394a90a200e
Type
HUMAN OTC DRUG
Nonproprietary name
ATROPA BELLADONNA - BRYONIA ALBA ROOT - BLACK COHOSH - ARABICA COFFEE BEAN - NITROGLYCERIN - IRIS VERSICOLOR ROOT - SODIUM CHLORIDE -
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
TRP Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2016-04-01
Substance
ARABICA COFFEE BEAN; ATROPA BELLADONNA; BLACK COHOSH; BRYONIA ALBA ROOT; IRIS VERSICOLOR ROOT; NITROGLYCERIN; SODIUM CHLORIDE
Active strength
3; 6; 6; 6; 6; 12; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vasodilation [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Migraine Headache Therapy
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ATROPA BELLADONNA3 [hp_X]/1
BRYONIA ALBA ROOT6 [hp_X]/1
BLACK COHOSH6 [hp_X]/1
ARABICA COFFEE BEAN6 [hp_X]/1
NITROGLYCERIN6 [hp_X]/1
IRIS VERSICOLOR ROOT12 [hp_X]/1
SODIUM CHLORIDE6 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
WQZ3G9PF0HInternal UNII lookup
T7J046YI2BInternal UNII lookup
K73E24S6X9Internal UNII lookup
3SW678MX72Internal UNII lookup
G59M7S0WS3Internal UNII lookup
X43D4L3DQCInternal UNII lookup
451W47IQ8XInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
317d3f42-783e-02b7-e054-00144ff88e88Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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95250459-30e4-45c1-b08a-993044f49109Product name220250805
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726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
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6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
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816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
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419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17312-041-14Migraine Headache Therapy1 in 1 PACKAGETABLET, ORALLY DISINTEGRATING14
17312-041-14Migraine Headache Therapy50 in 1 BOTTLETABLET, ORALLY DISINTEGRATING504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17312-041MIGRAINE HEADACHE THERAPY (ATROPA BELLADONNA - BRYONIA ALBA ROOT - BLACK COHOSH - ARABICA COFFEE BEAN - NITROGLYCERIN - IRIS VERSICOLOR ROOT - SODIUM CHLORIDE -) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]3Current NDC, Legacy NDC, 2 package rows20230111_317d3f42-783e-02b7-e054-00144ff88e88.zip

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 Headache TherapyATROPA BELLADONNA - BRYONIA ALBA ROOT - BLACK COHOSH - ARABICA COFFEE BEAN - NITROGLYCERIN - IRIS VERSICOLOR ROOT - SODIUM CHLORIDE -TRP Company317d3f42-783e-02b7-e054-00144ff88e882025-12-15WarningsExact identifier
ndc (product): 17312-041

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17312-041-14173120041141 BOTTLE in 1 PACKAGE (17312-041-14) / 50 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE1 bottle2016-04-010000-00-00NoNoCurrent