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

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Abropernol

Heel Inc

Abropernol Tablet


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

KEEP OUT OF REACH OF CHILDREN

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

ABROPERNOL INDICATIONS AND USAGE


  • Dermatitus
  • Minor skin irritations
  • Eczema, hyperhidrosis
  • Hyperkeratosis


WARNINGS

ABROPERNOL DOSAGE AND ADMINISTRATION

Adults and children above 6 years:
Infants and children to 6 years:

ACTIVE INGREDIENT

AbrotanumPulsatillaCalcarea fluoricaHamamelis virginianaAgaricus muscariusNitricum acidum 6X, Petroleum

INACTIVE INGREDIENT


PURPOSE

Abropernol

Abropernol

ARTEMISIA ABROTANUM FLOWERING TOP and PULSATILLA VULGARIS and CALCIUM FLUORIDE and HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK and AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY and NITRIC ACID and KEROSENE TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-6134
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARTEMISIA ABROTANUM FLOWERING TOP ARTEMISIA ABROTANUM FLOWERING TOP 4 [hp_X]
PULSATILLA VULGARIS PULSATILLA VULGARIS 4 [hp_X]
CALCIUM FLUORIDE Fluoride Ion 12 [hp_X]
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 4 [hp_X]
AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY AMANITA MUSCARIA VAR. MUSCARIA 5 [hp_X]
NITRIC ACID NITRIC ACID 6 [hp_X]
KEROSENE KEROSENE 6 [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:50114-6134-2 30000 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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Be sure to consult your doctor before taking any medication!
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