Fibromyalgia Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Fibromyalgia Relief

Apotheca Company

Fibromyalgia Relief




FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENS:  Aconitum napellus 30C, Arsenicum album 30C, Belladonna 30C, Conniinum 30C, Gelsemium sempervirens 30C, Hypericum perforatum 3X, 30C, Kali bichromicum 30C, Lacticum acidum 30C, Phosphoricum acidum 30C, Rhus toxicodendron 30C, Uricum acidum 30C.


Purpose

USES:  Temporarily relieves widespread aches, pains, and stiffness.


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.

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

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 State.


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.



INACTIVE INGREDIENTS:  Lactose, Magnesium stearate, Microcrystalline cellulose.


KEEP OUT OF REACH OF CHILDREN.  In case of overdose, get medical help or contact a Poison Control Center right away.


Uses

USES:  Temporarily relieves widespread aches, pains, and stiffness.



Dist. by:

The Magni Group, Inc.

McKinney, TX 75071 USA

www.magnilife.com

1-800645-9199



MAGNILIFE

NDC 57520-0582-1

Homeopathic

FIBROMYALGIA RELIEF

For widespread Aches, Pains and Stiffness

125 Tablets

Fibromyalgia Relief

Fibromyalgia Relief

Aconitum napellus, Arsenicum album, Belladonna, Coniinum, Gelsemium sempervirens, Hypericum perforatum, Kali bichromicum, Lacticum acidum, Phosphoricum acidum, Rhus toxicodendrom, Uricum acidum, TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57520-0582
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACONITUM NAPELLUS ACONITUM NAPELLUS 30 [hp_C]
ARSENIC TRIOXIDE ARSENIC TRIOXIDE 30 [hp_C]
ATROPA BELLADONNA ATROPA BELLADONNA 30 [hp_C]
CONIINE CONIINE 30 [hp_C]
GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]
Hypericum Perforatum HYPERICUM PERFORATUM 30 [hp_C]
POTASSIUM DICHROMATE DICHROMATE ION 30 [hp_C]
LACTIC ACID, DL- LACTIC ACID, DL- 30 [hp_C]
phosphoric acid PHOSPHORIC ACID 30 [hp_C]
TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF 30 [hp_C]
Uric Acid Uric Acid 30 [hp_C]

Inactive Ingredients

Ingredient Name Strength
LACTOSE
MAGNESIUM STEARATE
cellulose, microcrystalline

Product Characteristics

Color Size Imprint Code Shape
white 6 mm diamond; ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57520-0582-1 125 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-06-07


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Be sure to consult your doctor before taking any medication!
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