MIGRAINE RELIEF- not applicable tablet, orally disintegrating 
The Magni Company

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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DRUG FACTS

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

Migraine Relief

MIGRAINE RELIEF 
not applicable tablet, orally disintegrating
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43689-0010
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA6 [hp_X]  in 1 mg
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT6 [hp_X]  in 1 mg
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA3 [hp_X]  in 1 mg
BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9) BLACK COHOSH6 [hp_X]  in 1 mg
ARABICA COFFEE BEAN (UNII: 3SW678MX72) (ARABICA COFFEE BEAN - UNII:3SW678MX72) ARABICA COFFEE BEAN3 [hp_X]  in 1 mg
NITROGLYCERIN (UNII: G59M7S0WS3) (NITROGLYCERIN - UNII:G59M7S0WS3) NITROGLYCERIN12 [hp_X]  in 1 mg
IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (IRIS VERSICOLOR ROOT - UNII:X43D4L3DQC) IRIS VERSICOLOR ROOT6 [hp_X]  in 1 mg
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6 [hp_X]  in 1 mg
PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (PASSIFLORA INCARNATA FLOWERING TOP - UNII:CLF5YFS11O) PASSIFLORA INCARNATA FLOWERING TOP3 [hp_X]  in 1 mg
VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW) VALERIAN3 [hp_X]  in 1 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUND (convex) Size6mm
FlavorImprint Code ML
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43689-0010-21 in 1 CARTON07/17/201401/26/2023
1NDC:43689-0010-110800 mg in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/17/201401/26/2023
Labeler - The Magni Company (113501902)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(43689-0010) , api manufacture(43689-0010) , label(43689-0010) , pack(43689-0010)

Revised: 2/2022
 
The Magni Company