Aconitum Homaccord

Heel Inc

Aconitum Homaccord Oral Drop

FULL PRESCRIBING INFORMATION: CONTENTS*

• KEEP OUT OF REACH OF CHILDREN
• ACONITUM HOMACCORD INDICATIONS AND USAGE
• WARNINGS
• ACONITUM HOMACCORD DOSAGE AND ADMINISTRATION
• ACTIVE INGREDIENT
• INACTIVE INGREDIENT
• PURPOSE

FULL PRESCRIBING INFORMATION

KEEP OUT OF REACH OF CHILDREN

ACONITUM HOMACCORD INDICATIONS AND USAGE

• Fever
• Chills
• Cough
• Nausea
  

WARNINGS

ACONITUM HOMACCORD DOSAGE AND ADMINISTRATION

Adults and children above 11 years: 10 drops orally, 3 times daily, or as directed by a physician. Consult a physician for use in children under 12 years of age.

ACTIVE INGREDIENT

INACTIVE INGREDIENT

PURPOSE

Aconitum Homaccord ACONITUM NAPELLUS and EUCALYPTUS GLOBULUS LEAF and IPECAC LIQUID Product Information Product Type Human otc drug label Item Code (Source) NDC:50114-1180 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACONITUM NAPELLUS ACONITUM NAPELLUS 3 [hp_X] EUCALYPTUS GLOBULUS LEAF EUCALYPTUS GLOBULUS LEAF 2 [hp_X] Ipecac IPECAC 3 [hp_X] Inactive Ingredients Ingredient Name Strength ALCOHOL water Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50114-1180-4 50 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date 1986-01-31