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

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Chelidonium Homaccord

Biologische Heilmittel Heel

Chelidonium Homaccord 1.1ml Oral Vial


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT SECTION

Each 1.1 ml contains; Chelidonium majus 10X, 30X, 200X 6.6 mcl each; Belladonna 10X, 30X, 200X, 1000X 3.3 mcl each.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of the reach of children.

PREGNANCY OR BREAST FEEDING

Pregnancy and nursing mothers: Pregnancy Category C. In general, homeopathic drugs are not known to cause direct or indirect harm to the fetus. However, animal reproduction studies have not been performed and there are no well-controlled studies in pregnant women. In cases of pregnancy or suspected pregnancy, a physician should be consulted before administering this drug. It is not known whether any of the ingredients are excreted in human milk. However because many drugs are excreted in human milk, homeopathic drugs should be administered with caution to nursing mothers.



CHELIDONIUM HOMACCORD INDICATIONS AND USAGE

For the temporary relief of abdominal discomfort such as:

  • Bloating
  • Spasms
  • Colic and flatulence
  • Constipation or diarrhea

WARNINGS

If symptoms persist for more than a few days, a physician should be consulted.

CHELIDONIUM HOMACCORD DOSAGE AND ADMINISTRATION

Oral liquid in vials.

Admistration: NOT FOR INJECTION - FOR ORAL ADMINISTRATION ONLY.

INACTIVE INGREDIENT

Isotonic sodium chloride solution

PURPOSE


Chelidonium Homaccord

Chelidonium Homaccord.jpg

Chelidonium Homaccord

CHELIDONIUM MAJUS and ATROPA BELLADONNA SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51885-4996
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CHELIDONIUM MAJUS CHELIDONIUM MAJUS 10 [hp_X]
ATROPA BELLADONNA ATROPA BELLADONNA 10 [hp_X]

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51885-4996-1 1.1 in 1 AMPULE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-02-17


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Be sure to consult your doctor before taking any medication!
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