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

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Scrofularoforce

Apotheca Company

Scrofularoforce




FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENTS:  Juniperus virginiana 3X, Rumex crispus 3X, Scrophularia nodosa 3X, Xanthoxylum fraxineum 3X, Lymph node 8X, Baryta carbonica 12X, Baryta muriatica 12X, Belladonna 12X, Calcarea carbonica 12X, Conium maculatum 12X, Helleborus niger 12X, Iodium 12X, Kali phosphoricum 12X, Lachesis mutus 12X, Natrum phosphoricum 12X, Silicea 12X.


Purpose

INDICATIONS:  For temporary relief of constricted feeling of the chest, palpitations with anxiety, purplish hue, burning, stinging pains, inflammation of connective tissues.


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 constricted feeling of the chest, palpitations with anxiety, purplish hue, burning, stinging pains, inflammation of connective tissues.





Distributed By:

BIOACTIVE NUTRITIONAL

Melbourne, FL 32935


For Nutritional Information write:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935


BioActive Homeopathic

SCROFULAROFORCE

1 FL OZ (30 ml)

Scrofularoforce


Scrofularoforce

Juniperus virginiana, Rumex crispus, Scrophularia nodosa, Xanthoxylum fraxineum, Lymph node, Baryta carbonica, Baryta muriatica, Belladonna, Calcarea carbonica, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57520-0612
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
JUNIPERUS VIRGINIANA TWIG JUNIPERUS VIRGINIANA TWIG 3 [hp_X]
RUMEX CRISPUS ROOT Rumex Crispus Root 3 [hp_X]
SCROPHULARIA NODOSA SCROPHULARIA NODOSA 3 [hp_X]
ZANTHOXYLUM AMERICANUM BARK ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]
SUS SCROFA LYMPH SUS SCROFA LYMPH 8 [hp_X]
BARIUM CARBONATE BARIUM CATION 12 [hp_X]
Barium Chloride Dihydrate BARIUM CATION 12 [hp_X]
ATROPA BELLADONNA ATROPA BELLADONNA 12 [hp_X]
OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]
Conium Maculatum Flowering Top CONIUM MACULATUM FLOWERING TOP 12 [hp_X]
HELLEBORUS NIGER ROOT HELLEBORUS NIGER ROOT 12 [hp_X]
Iodine IODINE 12 [hp_X]
potassium phosphate, dibasic PHOSPHATE ION 12 [hp_X]
LACHESIS MUTA VENOM LACHESIS MUTA VENOM 12 [hp_X]
SODIUM PHOSPHATE, DIBASIC ANHYDROUS 12 [hp_X]
SILICON DIOXIDE 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57520-0612-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-02-14


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Be sure to consult your doctor before taking any medication!
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