CACTUS COMPOSITUM - crataegus laevigata fruit, selenicereus grandiflorus stem, potassium dichromate, spigelia anthelmia and nitroglycerin solution 
Heel Inc

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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Cactus compositum oral vial

DESCRIPTION

Each 2.2 ml ampule contains: 

Ingredient Name

Potency

Quantity

Crataegus oxyacantha

2x

22µ

Cactus grandflorus

3x

22µ

Kali carbonicum

5x

22µ

Spigelia anthelmia

5x

22µ

Glonoinum

5x

13.2µ


Inactive Ingredient: Isotonic Sodium Chloride solution

INDICATION AND USAGE

Cactus compositum® Oral Vials is a homeopathic drug product indicated for the ancillary treatment of coronary circulatory disorders, angina pectoris and myocardial weakness

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

CONTRAINDICATIONS

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

WARNINGS AND PRECAUTIONS

Warnings and Precautions

None

ADVERSE REACTIONS

No adverse events have been reported with a causal relationship to Cactus 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 Cactus compositum® Oral Vials is not fully understood.

Pharmacodynamics

Not applicable for homeopathic medicinal products.

DOSAGE

1 oral vial containing 2.2ml solution for oral administration

Cactus compositum oral vial.jpg

CACTUS COMPOSITUM 
crataegus laevigata fruit, selenicereus grandiflorus stem, potassium dichromate,spigelia anthelmia, and nitroglycerin solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:50114-5120
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CRATAEGUS LAEVIGATA FRUIT (CRATAEGUS LAEVIGATA FRUIT) CRATAEGUS LAEVIGATA FRUIT2 [hp_X]  in 2.2 mL
SELENICEREUS GRANDIFLORUS STEM (SELENICEREUS GRANDIFLORUS STEM) SELENICEREUS GRANDIFLORUS STEM3 [hp_X]  in 2.2 mL
POTASSIUM DICHROMATE (DICHROMATE ION) POTASSIUM DICHROMATE5 [hp_X]  in 2.2 mL
SPIGELIA ANTHELMIA (SPIGELIA ANTHELMIA) SPIGELIA ANTHELMIA5 [hp_X]  in 2.2 mL
NITROGLYCERIN (NITROGLYCERIN) NITROGLYCERIN5 [hp_X]  in 2.2 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50114-5120-610 in 1 CARTON
12.2 mL in 1 AMPULE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/31/1993
Labeler - Heel Inc (102783016)

Revised: 12/2013
 
Heel Inc