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

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Rheumaforce

Apotheca Company

Rheumaforce




FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENTS:  Chondrus crispus 3X, Cimicifuga racemosa 3X, Spiraea ulmaria 3X, Symphytum officinale 3X, Trifolium pratense 3X, Urtica urens 3X, Xanthoxylum fraxineum 3X, Colchicum autumnale 12X, Ferrum phosphoricum 12X, Formica rufa 12X, Lithium carbonicum 12X, Natrum sulphuricum 212X, Rhododendron chrysanthum 12X, Rhus toxicodendron 12X.

Purpose

INDICATIONS:  For temporary relief of pains throughout shoulder joint, arm, fingers, and small joints generally; swelling and tenderness of the finger and toe joints; and swellings in the joints with inflammation.

WARNINGS:  If pregnant or breast-feeding, ask a health care professional before use.

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

Do not use if tamper evident seal is broken or missing.  Store in a cool, dry place.

DIRECTIONS:  10 drops orally, 3 times a day.  Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.


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


Uses

INDICATIONS:  For temporary relief of pains throughout shoulder joint, arm, fingers, and small joints generally; swelling and tenderness of the finger and toe joints; and swellings in the joints with inflammation.


Distributed by:

BIOACTIVE NUTRITIONAL

Melbourne, FL 32935


For Nutritional Information write:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935


BioActive Homeopathic

RHEUMAFORCE

1 FL OZ (30 ml)

Rheumaforce

Rheumaforce

Chondrus crispus, Cimicifuga racemosa, Spiraea ulmaria, Symphytum officinale, Trifolium pratense, Urtica urens, Xanthoxylum fraxineum, Colchicum autumnale, Ferrum phosphoricum, Formica rufa, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57520-0704
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CHONDRUS CRISPUS 3 [hp_X]
BLACK COHOSH BLACK COHOSH 3 [hp_X]
FILIPENDULA ULMARIA ROOT FILIPENDULA ULMARIA ROOT 3 [hp_X]
COMFREY ROOT COMFREY ROOT 3 [hp_X]
TRIFOLIUM PRATENSE FLOWER 3 [hp_X]
Urtica Urens URTICA URENS 3 [hp_X]
ZANTHOXYLUM AMERICANUM BARK ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]
COLCHICUM AUTUMNALE BULB COLCHICUM AUTUMNALE BULB 12 [hp_X]
FERRUM PHOSPHORICUM FERRUM PHOSPHORICUM 12 [hp_X]
FORMICA RUFA Formica Rufa 12 [hp_X]
LITHIUM CARBONATE LITHIUM CATION 12 [hp_X]
SODIUM SULFATE SODIUM CATION 12 [hp_X]
RHODODENDRON AUREUM LEAF RHODODENDRON AUREUM LEAF 12 [hp_X]
TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57520-0704-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-05-24


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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