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

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Cutis compositum

Heel Inc

Cutis compositum oral vial


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

CUTIS COMPOSITUM DESCRIPTION

Each 2.2 ml ampule contains: 

Ingredient Name

Potency

Quantity

Aesculus hippocastanum

6x

22µ

a-Ketoglutaricum acidum

10x

22µ

Calcarea fluorica

13x

22µ

Cortisone aceticum

28x

22µ

Cutis suis

8x

22µ

Formicum acidum

10x

22µ

Fumaricum acidum

198x

22µ

Funiculus umbilicals suis

10x

22µ

Galium aparine

6x

22µ

Glandula suprarenalis

10x

22µ

Hepar suis

10x

22µ

Ichthyolum

28x

22µ

Ignatia amara

6x

22µ

Lappa major

6x

22µ

Ledum palustre

4x

22µ

Mercurius solubilis

13x

22µ

Natrum oxalaceticum

10x

22µ

Phosphoricum acidum

6x

22µ

Placenta suis

10x

22µ

Selinium metallicum

10x

22µ

Splen suis

10x

22µ

Sulfur

10x

22µ

Thallium sulphuricum

13x

22µ

Thuja occidentalis

8x

22µ

Urtica urens

4x

22µ


Inactive Ingredient: Isotonic Sodium Chloride solution

INDICATION AND USAGE

Cutis compositum® Oral Vials is a homeopathic drug product is indicated for the temporary relief of persistent skin conditions such as acne, eczema, and allergic dermatitis

CUTIS 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

CUTIS COMPOSITUM CONTRAINDICATIONS

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

WARNINGS AND PRECAUTIONS

Warnings and Precautions

None

CUTIS COMPOSITUM ADVERSE REACTIONS

No adverse events have been reported with a causal relationship to Cutis 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 Cutis 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

Cutis compositum

Cutis compositum

LEDUM PALUSTRE TWIG, URTICA URENS, AESCULUS HIPPOCASTANUM FLOWER, GALIUM APARINE, STRYCHNOS IGNATII SEED, ARCTIUM LAPPA ROOT, PHOSPHORIC ACID, SUS SCROFA SKIN, THUJA OCCIDENTALIS LEAFY TWIG, FUMARIC ACID,SUS SCROFA UMBILICAL CORD,SUS SCROFA ADRENAL GLAND,PORK LIVER,.ALPHA.-KETOGLUTARIC ACID, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,SELENIUM,SUS SCROFA SPLEEN,SULFUR,CALCIUM FLUORIDE, MERCURIUS SOLUBILIS,THALLIUM SULFATE,CORTISONE ACETATE, ICHTHAMMOL, FORMIC ACID, SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:50114-5170
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG 4 [hp_X]
Urtica Urens URTICA URENS 4 [hp_X]
AESCULUS HIPPOCASTANUM FLOWER AESCULUS HIPPOCASTANUM FLOWER 6 [hp_X]
GALIUM APARINE GALIUM APARINE 6 [hp_X]
STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED 6 [hp_X]
ARCTIUM LAPPA ROOT ARCTIUM LAPPA ROOT 6 [hp_X]
phosphoric acid PHOSPHORIC ACID 6 [hp_X]
SUS SCROFA SKIN SUS SCROFA SKIN 8 [hp_X]
THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG 8 [hp_X]
FUMARIC ACID FUMARIC ACID 10 [hp_X]
SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD 10 [hp_X]
SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND 10 [hp_X]
PORK LIVER PORK LIVER 10 [hp_X]
.ALPHA.-KETOGLUTARIC ACID .alpha.-ketoglutaric Acid 10 [hp_X]
SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE 10 [hp_X]
SUS SCROFA PLACENTA SUS SCROFA PLACENTA 10 [hp_X]
Selenium SELENIUM 10 [hp_X]
SUS SCROFA SPLEEN SUS SCROFA SPLEEN 10 [hp_X]
SULFUR SULFUR 10 [hp_X]
CALCIUM FLUORIDE Fluoride Ion 13 [hp_X]
MERCURIUS SOLUBILIS MERCURIUS SOLUBILIS 13 [hp_X]
CORTISONE ACETATE CORTISONE 28 [hp_X]
THALLIUM SULFATE SULFATE ION 13 [hp_X]
ICHTHAMMOL ICHTHAMMOL 28 [hp_X]
Formic Acid 198 [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:50114-5170-6 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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