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Cor compositum

Heel Inc

Cor compositum oral vial


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

COR COMPOSITUM DESCRIPTION

Each 2.2 ml ampule contains: 

Ingredient

Potency

Quantity

alpha-Ketoglutaricum acidum

6X

22µ

Arnica montana, radix

4X

22µ

Arsenicum album

8X

22µ

Carbo vegetabilis

18X

22µ

Cactus grandiflorus 

3X 

22µ

Cor suis

8X

22µ

Crataegus oxyacantha

6X

22µ

Fumaricum acidum

8X

22µ

Glonoinum

4X

22µ

Hepar suis

8X

22µ

Ignatia amara

6X

22µ

Kali carbonicum

4X

22µ

Kalmia latifolia

4X

22µ

Malicum acidum

8X

22µ

Naja tripudians

10X

22µ

Natrum oxalaceticum

8X

22µ

Quabain

8X

22µ

Ranunculus bulbosus

6X

22µ

Sarcolacticum acidum

6X

22µ

Spigelia anthelmia

22µ


Inactive Ingredient: Isotonic Sodium Chloride solution

INDICATION AND USAGE

Cor compositum® Oral Vial is a homeopathic drug indicated for the use as an adjunct to standard medical treatment of coronary disorders such as myocardial insufficiency, angina pectoris, and hypertension

COR COMPOSITUM DOSAGE AND ADMINISTRATION

Dosage:

Adults and children above 6 years: 1 vial orally 1-3 times daily

Children up to 6 years: ½ vial orally 1-3 times daily

COR COMPOSITUM CONTRAINDICATIONS

* Cor compositom® Oral Vials are contraindicated in patients with known hypersensitivity to Cor compositum® or any of its ingredients

WARNINGS AND PRECAUTIONS

Warnings and Precautions

None

COR COMPOSITUM ADVERSE REACTIONS

No adverse events have been reported with a causal relationship to Cor compositum® Oral Vials

OVERDOSAGE

Overdosage: No negative effects of an overdose have been reported and none are expected due to the homeopathic dilutions

CLINICAL PHARMACOLOGY

Mechanism of Action

The exact mechanism of Cor compositum® Oral Vials is not fully understood.

Pharmacodynamics

Not applicable for homeopathic medicinal products.

DOSAGE

1 oral vial containing 2.2 ml solution for oral administration

Cor compositum

Cor compositum

SELENICEREUS GRANDIFLORUS STEM, ARNICA MONTANA ROOT, NITROGLYCERIN,POTASSIUM CARBONATE, KALMIA LATIFOLIA LEAF, CRATAEGUS LAEVIGATA FRUIT,STRYCHNOS IGNATII SEED, RANUNCULUS BULBOSUS, LACTIC ACID, L-,ARSENIC TRIOXIDE, PORK HEART, FUMARIC ACID, PORK LIVER,.ALPHA.-KETOGLUTARIC ACID, MALIC ACID, SODIUM DIETHYL OXALACETATE, OUABAIN, NAJA NAJA VENOM,SPIGELIA ANTHELMIA and ACTIVATED CHARCOAL SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:50114-1058
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SELENICEREUS GRANDIFLORUS STEM SELENICEREUS GRANDIFLORUS STEM 3 [hp_X]
ARNICA MONTANA ROOT ARNICA MONTANA ROOT 4 [hp_X]
nitroglycerin NITROGLYCERIN 4 [hp_X]
POTASSIUM CARBONATE CARBONATE ION 4 [hp_X]
kalmia latifolia leaf KALMIA LATIFOLIA LEAF 4 [hp_X]
CRATAEGUS LAEVIGATA FRUIT CRATAEGUS LAEVIGATA FRUIT 6 [hp_X]
STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED 6 [hp_X]
Ranunculus Bulbosus Ranunculus Bulbosus 6 [hp_X]
LACTIC ACID, L- LACTIC ACID, L- 6 [hp_X]
ARSENIC TRIOXIDE ARSENIC TRIOXIDE 8 [hp_X]
PORK HEART PORK HEART 8 [hp_X]
FUMARIC ACID FUMARIC ACID 8 [hp_X]
PORK LIVER PORK LIVER 8 [hp_X]
.ALPHA.-KETOGLUTARIC ACID .alpha.-ketoglutaric Acid 8 [hp_X]
Malic Acid 8 [hp_X]
OUABAIN OUABAIN 8 [hp_X]
NAJA NAJA VENOM Naja Naja Venom 10 [hp_X]
SPIGELIA ANTHELMIA SPIGELIA ANTHELMIA 10 [hp_X]
Activated Charcoal ACTIVATED CHARCOAL 18 [hp_X]

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 2.2 in 1 AMPULE
2 NDC:50114-1058-6 10 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1993-01-31


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