The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active ingredient (in each drops)Menthol 5.4mg
Otc - Purpose
PurposeCough suppressant/Oral anesthetic
Indications & Usage
Uses temporarily relieves:
cough as may occur with a coldoccasional minor irritation and sore throat
WarningsSore 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. If sore mouth symptoms do not improve in 7 days, see yourdentist or doctor promptly. These symptoms may be serious.
Otc - Ask Doctor
- Ask a doctor before use if you have: persistent or chronic cough such as occurs with smoking, asthma, or emphysemacough accompanied by excessive phlegm (mucus)
Otc - Stop Use
- Stop use and ask doctor ifcough 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 worsenssore mouth does not improve in 7 days
Otc - Pregnancy Or Breast Feeding
If pregnant or breast-feeding, ask a health professional before use.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Dosage & Administration
Directionsadults and children 5 years and over - dissolve 1 lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.children under 5 years - ask a doctor
Other Safety Information
- Other information 10 calories per dropdo not use if bag is torn or open
Inactive ingredients: Corn starch, corn syrup, eucalyptus oil, FD&C blue no. 1, FD&C red no. 40, glycerin, gum arabic, medium chain triglycerides, natural flavors, potassium sorbate, soybean oil, sucrose and water.
Otc - Questions
Questions? Or to report an adverse event call 1-800-245-2898. Monday - Friday, 9AM to 4PM EST
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