Menthol Vapor Cough Drops

The listing

NDC product code

72628-108 (labeller 72628, product 108)

Labeller

BOSTON NUTRACEUTICAL PRODUCTION, S.L

Brand name

Menthol Vapor Cough Drops

Generic name

Menthol

Dosage form

Pastille

Route

oral

Marketing category

OTC MONOGRAPH DRUG M012

Marketing start

1 June 2020

Listing expires

31 December 2026

RxNorm concept

1995300

Active ingredients

Strengths as listed in the FDA National Drug Code Directory, retrieved 4 September 2026. "Other listings" counts every other product on this site containing the same ingredient at any strength.

What the label claims

These are read from this product's own label, not assigned by us and not inferred from the ingredient.

Stated purposeOral anesthetic

Stated useSore throatMinor throat irritationSore mouth, gums and canker sores

Drug Facts, as filed

Quoted from the label FDA holds for this product. Long fields are truncated. The panel printed on the package you are holding is the one that governs.

Active ingredient

in each drop Purposes Menthol 20 mg Severe Menthol Caugh Suppressant Oral Anesthetic

Purpose

Temporarily relieves ocassional minor irritation and pain due to: sore throat sore mouth

Uses

Purposes Temporarily relieves ocassional minor irritation and pain due to: sore throat sore mouth

Warnings

Sore throat warning: severe or persistent throat accompanied by high fever headache, nausea and vomiting maybe serious. Consult a doctor promptly. Do not use more than 2 days or administer to children under 12 years of old.

Ask a doctor before use

A severe throat accompanied by difficulty in breathing or that last more than 2 days A severe throat accompanied by fever, headache, rash, swealling, nausea or vomiting.

Stop use and ask a doctor if

Stop use and consult doctor if sore mouth symptons does not improve in 7 days or if irritation, pain or redness persists or worse If pregnant or breast feeding, ask a health professional before use.

If pregnant or breast-feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

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

Directions

Adults and children 12 years and over: dissolve 1 drop slowly in mouth. Repeated every two hours as needed or as directed by a doctor. Children 12 years or under do not use

Inactive ingredients

corn syrup, sucrose, water, eucalyptus oil, acacia, FD&Blue No.1 Back Label

Other information

or comments call: 1-888-423-0139

Label version 3, effective 7 October 2024. Retrieved from the openFDA drug label API on 4 September 2026. Read the full label on DailyMed.

Packages

The package NDC adds a third segment to the product code, identifying the pack size. See how to read an NDC.

Identical on the active ingredient

One other listing states exactly the same active ingredient at exactly the same strength in the same dosage form. They are not necessarily the same product: inactive ingredients, flavour and pack size differ, and this site does not compare prices.

Sources for this page

• FDA National Drug Code Directory entry for 72628-108
• DailyMed label, set id a7062db1-8201-b400-e053-2a95a90a55e8
• How Lozenges builds these pages