Menthol Cough Drops Honey Lemon Flavor MENTHOL HONEY LEMON FLAVOR CVS PHARMACY FDA Approved Uses temporarily relieves: cough as may occur with a cold ocassional minor irritation and sore throat
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Substance Menthol
Route
ORAL
Applications
M012
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
Active Ingredient: Menthol 7.6 mg.............cough suppresant/ oral anesthetic
Inactive Ingredients
citric acid eucalyptus oil isomalt natural favors stevia turmeric (coloring) Front Label
Strengths
7.6 mg
Treats Conditions
Uses Temporarily Relieves Cough As May Occur With A Cold Ocassional Minor Irritation And Sore Throat
Pill Appearance
Shape: oval Color: yellow Imprint: None

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UPC
0050428137000
UNII
L7T10EIP3A
Packaging

Back label

Package Descriptions
  • Back label

Overview

Uses temporarily relieves: cough as may occur with a cold ocassional minor irritation and sore throat

Indications & Usage

Uses temporarily relieves: cough as may occur with a cold ocassional minor irritation and sore throat

Dosage & Administration

Directions Adults and children 6 years and over: dissolve 1 drop slowly in the mouth. Repeated every 2 hours as needed or as directed by a doctor. Children under 6 years: as a doctor

Warnings & Precautions
Warnings Sore throat warning: severe or persistence sore throat accompanied by high fever, headache, nausea and vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days.
Purpose

Uses temporarily relieves: cough as may occur with a cold ocassional minor irritation and sore throat

Stop Use & Ask a Doctor

Stop and consult a doctor before use if cough persist 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 mouth symptoms do not improve in 7 days, or if irritation, pain or redness persists or worsens.

Keep Out of Reach of Children

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

Questions

Questions? or to report and adverse event call: 1-833-552-1767


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