Meijer Severe Menthol Throat Drops

The listing

NDC product code

79481-0092 (labeller 79481, product 0092)

Labeller

Meijer

Brand name

Meijer Severe Menthol Throat Drops

Generic name

Menthol

Dosage form

Lozenge

Route

oral

Marketing category

OTC MONOGRAPH DRUG M012

Marketing start

18 April 2024

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 throatSore 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) Menthol 20 mg

Purpose

Oral anesthetic

Uses

temporarily relieves: occasional minor iritation and pain associated with sore throat and sore mouth

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. Do not use more than 2 days or administer to children under 12 years of age.

Ask a doctor before use

a severe sore throat accompanied by difficulty in breathing or that lasts 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 doctor if sore mouth does not improve in 7 days irritation, pain or redness persists or worsens

If pregnant or breast-feeding

, ask a health professional before use.

Keep out of reach of children

Keep out of reach of children.

Directions

adults and children 12 years and over - dissolve 1 drop slowly in mouth. Repeat every two hours as needed or as directed by a doctor. children 12 years and under - do not use

Inactive ingredients

Corn starch, corn syrup, eucalyptus oil, FD&C blue no. 1, glycerin, gum arabic, medium chain triglycerides, potassium sorbate, soybean oil, sucrose and water.

Other information

Or to report an adverse event call 1-800-245-2898 , Monday - Friday, 9AM to 4PM EST

Label version 3, effective 18 December 2025. 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

13 other listings state exactly the same active ingredient at exactly the same strength in the same dosage form, across 5 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 79481-0092
• DailyMed label, set id 16603ca4-1ce5-2e7e-e063-6394a90ad6f1
• How Lozenges builds these pages