MIGRAINE RELIEF- not applicable tablet, orally disintegrating

Migraine Relief by

Drug Labeling and Warnings

Migraine Relief by is a Homeopathic medication manufactured, distributed, or labeled by The Magni Company, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Belladonna 6X, 12X, Bryonia (alba) 6X, 12X, 18X, Chamomilla 3X, Cimicifuga Racemosa 6X, 12X, 18X, Passiflora Incarnata 3X, Valeriana Officinalis 3X

USES

Temporarily relieves acute symptoms of migraine headaches such as

pressure, pulsating, stabbing headache, blurred vision, vertigo, nausea, sensitivity 

WARNINGS:

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.

This product is intended to complement proper medical attention.

If symptoms persist for more than 7 days or worsen, consult your physician.

Other Information

Store tightly closed in a cool, dry place (59 - 86F).

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

Pharmacopeia of the United States.

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

DIRECTIONS:

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

USES

Temporarily relieves acute symptoms of migraine headaches such as

pressure, pulsating, stabbing headache, blurred vision, vertigo, nausea, sensitivity 

INACTIVE INGREDIENTS:

Lactose, Magnesium Stearate, Microcrystaline Cellulose.

QUESTIONS:

Distributed by:

The Magni Group, Inc.

Mckinney, TX 75074 USA

www.magnilife.com

1-800-645-9199

PACKAGE LABEL DISPLAY:

MAGNILIFE    Homeopathic

    Since 1999    NDC: 43689-0010-1  

MIRGRAINE RELIEF

RELIEVES SYMPTOMS OF MIGRAINE HEADACHES

Headache, Sensitivity, Vertigo Nausea, Blurred Vision

90 Tablets

INGREDIENTS AND APPEARANCE

MIGRAINE RELIEF 
not applicable tablet, orally disintegrating

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43689-0010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H)	ATROPA BELLADONNA	6 [hp_X]  in 1 mg
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	6 [hp_X]  in 1 mg
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ)	MATRICARIA RECUTITA	3 [hp_X]  in 1 mg
BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9)	BLACK COHOSH	6 [hp_X]  in 1 mg
ARABICA COFFEE BEAN (UNII: 3SW678MX72) (ARABICA COFFEE BEAN - UNII:3SW678MX72)	ARABICA COFFEE BEAN	3 [hp_X]  in 1 mg
NITROGLYCERIN (UNII: G59M7S0WS3) (NITROGLYCERIN - UNII:G59M7S0WS3)	NITROGLYCERIN	12 [hp_X]  in 1 mg
IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (IRIS VERSICOLOR ROOT - UNII:X43D4L3DQC)	IRIS VERSICOLOR ROOT	6 [hp_X]  in 1 mg
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	6 [hp_X]  in 1 mg
PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (PASSIFLORA INCARNATA FLOWERING TOP - UNII:CLF5YFS11O)	PASSIFLORA INCARNATA FLOWERING TOP	3 [hp_X]  in 1 mg
VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW)	VALERIAN	3 [hp_X]  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)

Product Characteristics
Color	white	Score	no score
Shape	ROUND (convex)	Size	6mm
Flavor		Imprint Code	ML
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43689-0010-2	1 in 1 CARTON
1	NDC: 43689-0010-1	10800 mg in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/17/2014

Labeler - The Magni Company (113501902)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43689-0010) , api manufacture(43689-0010) , label(43689-0010) , pack(43689-0010)