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

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Belladonna compositum

Heel Inc


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

KEEP OUT OF REACH OF CHILDREN

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

NDICATIONS AND USAGE


  • Edema
  • Suppuration
  • Pain

WARNINGS


BELLADONNA COMPOSITUM DOSAGE AND ADMINISTRATION

Adults and children above 6 years: 1 tablet sublingually or dissolved completely in mouth 3 times daily or as directed by a physician. Infants and children to 6 years: 1/2 the adult dosage.

ACTIVE INGREDIENT

Each 300 mg tablet contains as active ingredients: Belladonna 4X, Dulcamara 4X, Hepar sulphuris calcareum 6X, Apis mellifica 4x, Arnica montana, radix 4X, Phytolacca decandra 4X, Mercuris cynatus 8X

INACTIVE INGREDIENT


PURPOSE

Belladonna compositumEnter section text here

Belladonna compositum

ATROPA BELLADONNA and SOLANUM DULCAMARA TOP and CALCIUM SULFIDE and APIS MELLIFERA and ARNICA MONTANA and PHYTOLACCA AMERICANA ROOT and MERCURIC CYANIDE and TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-6025
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ATROPA BELLADONNA ATROPA BELLADONNA 4 [hp_X]
Solanum Dulcamara Top Solanum Dulcamara Top 4 [hp_X]
CALCIUM SULFIDE CALCIUM CATION 6 [hp_X]
APIS MELLIFERA APIS MELLIFERA 4 [hp_X]
ARNICA MONTANA ARNICA MONTANA 4 [hp_X]
PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT 4 [hp_X]
Mercuric Cyanide MERCURIC CYANIDE 8 [hp_X]

Inactive Ingredients

Ingredient Name Strength
LACTOSE
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
white 9 mm Heel ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50114-6025-2 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1984-01-31


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