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

Psorinoheel

Heel Inc

Psorinoheel oral vial

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DESCRIPTION

Each1.1 ml ampule contains: 

Ingredient Name

Potency

Quantity

Bacillinum

12x

0.55µ

Bufo rana

10x

1.1µ

Cictuta virosa

5x

0.55µ

Kali bismuthum iodatum

5x

0.55 µ

Medorrhinum

12x

1.1µ

Natrum muriaticum

12x

1.1µ

Oleander

4x

0.55µ

Psorinum

10x

1.1µ

Sulphur

6x

1.1µ

Thuja occidentalis

6x

1.1µ

Vaccinotoxinum

8x

1.1µ


Inactive Ingredient: Isotonic Sodium Chloride solution

INDICATION AND USAGE

Psorinoheel® Oral Vials is a homeopathic drug product indicated for the stimulation of the defense mechanism in chronic skin disorders, hepatic damage , and chronic illness

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

Contraindications

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

WARNINGS AND PRECAUTIONS

Warnings and Precautions

None

ADVERSE REACTIONS

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

Pharmacodynamics

Not applicable for homeopathic medicinal products.

DOSAGE

1 oral vial containing 1.1 ml solution for oral administration

Psorinoheel

SULFUR, THUJA OCCIDENTALIS LEAFY TWIG, VACCINIA VIRUS STRAIN NEW YORK CITY BOARD, GONORRHEAL URETHRAL SECRETION HUMAN,SODIUM CHLORIDE, NERIUM OLEANDER LEAF,CICUTA VIROSA ROOT, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:50114-5324
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SULFUR SULFUR 6 [hp_X]
THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]
VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN 8 [hp_X]
BUFO BUFO CUTANEOUS GLAND BUFO BUFO CUTANEOUS GLAND 10 [hp_X]
SCABIES LESION LYSATE (HUMAN) SCABIES LESION LYSATE (HUMAN) 10 [hp_X]
GONORRHEAL URETHRAL SECRETION HUMAN GONORRHEAL URETHRAL SECRETION HUMAN 12 [hp_X]
Nerium Oleander Leaf NERIUM OLEANDER LEAF 4 [hp_X]
CICUTA VIROSA ROOT CICUTA VIROSA ROOT 5 [hp_X]
POTASSIUM DICHROMATE DICHROMATE ION 5 [hp_X]

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 1.1 in 1 AMPULE
2 NDC:50114-5324-6 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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