FDA Label for Broncolin Honey Eucalyptus
View Indications, Usage & Precautions
Broncolin Honey Eucalyptus Product Label
The following document was submitted to the FDA by the labeler of this product Broncolin, S.a. De C.v.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Menthol 7.5mg
Purpose
Cough Suppressant/Oral Anesthetic
Uses
temporarily relieves •Cough due to minor and bronchial irritation occurring with a cold or inhaled irritants •occasional minor irritation and sore throat
Warnings
Sore throat warning: If sore throat is severe •persists for more than 2 days • is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These symptoms may be serious.
Ask A Doctor Before Use If You Have
•persistent or chronic cough such as occurs with smoking, asthma, or emphysema •cough accompanied by excessive phlegm (mucus)
When Using This Product
•do not exceed recommended dosage
Stop Use And Ask A Doctor If
•cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. •sore throat is severe or irritation, pain, or redness lasts or worsens •sore mouth does not improve in 7 days.
Keep Out Of Reach Of Children
if pregnant or breast feeding ask a Health Professional before using
Directions
• adults and children 6 years and older: dissolve 1 drop slowly in the mouth. May be repeated every hour as needed or as directed by a doctor • children under 6 years: ask a doctor.
Inactive Ingredients
Citric Acid, Elderberry flower extract, Eucalyptus leaf extract, Eucalyptus oil leaf extract, Glucose, Honey, Mullein flower extract, Sugar
Package Label
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