Honey Lemon Menthol Cough Drops

The listing

NDC product code

76162-024 (labeller 76162, product 024)

Labeller

Topco Associates LLC

Brand name

Honey Lemon Menthol Cough Drops

Generic name

Honey Lemon Menthol

Dosage form

Pastille

Route

oral

Marketing category

OTC MONOGRAPH DRUG M012

Marketing start

8 June 2023

Listing expires

31 December 2026

RxNorm concept

1250189

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 purposeCough suppressantOral anesthetic

Stated useSore throatMinor throat irritationCough

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

7.5 mg Cough Suppressant Oral anesthetic Front Panel

Purpose

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

Uses

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

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 or administer to children under 12 years of age.

Ask a doctor before use

a severe throat accompanied by difficulty in breathing or that last more than 2 days a sore throat accompanied by fever, headache, rash, swelling, nausea or vomiting

Stop use and ask a doctor if

Stop use and consult a doctor if sore mouth symptons do not improve in 7 days or if irritation, pains or redness persists or worsens.

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 2 hours as needed or as directed by a doctor. Children under 12 years and under do not use

Inactive ingredients

citric acid, honey, flavors, glucose syrup, sucrose, turmeric

Other information

or to report and adverse event call: 1-800-423-0139

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

10 other listings state exactly the same active ingredient at exactly the same strength in the same dosage form, across 7 different labellers. 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 76162-024
• DailyMed label, set id f5be283b-524d-26af-e053-2995a90a3972
• How Lozenges builds these pages