EXTRA STRENGTH WITH NATURAL MENTHOL GLACIER MINT COUGH SUPPRESSANT

The listing

NDC product code

63667-503 (labeller 63667, product 503)

Labeller

Ricola USA Inc.

Brand name

EXTRA STRENGTH WITH NATURAL MENTHOL GLACIER MINT COUGH SUPPRESSANT

Generic name

MENTHOL

Dosage form

Lozenge

Route

oral

Marketing category

OTC MONOGRAPH DRUG M012

Marketing start

27 May 2013

Listing expires

31 December 2026

RxNorm concept

1424614

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 suppressant

Stated useCough

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, 8.3 mg

Purpose

Purpose Cough suppressant

Uses

temporarily relieves: cough due to minor throat and bronchial irritation occurring with a cold or inhaled irritants

Warnings

Warnings

Ask a doctor before use

Ask doctor before use if you have persistent chronic cough such as occurs with smoking, asthma, or emphysema cough accompanied by excessive phlegm (mucus)

Stop use and ask a doctor if

cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition

Keep out of reach of children

Keep out of reach of children.

Directions

adults and children 6 years and older: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed or as directed by a doctor children under 6 years: ask a doctor

Inactive ingredients

extracts of peppermint and a Ricola herb mixture (elder, horehound, hyssop, lemon balm, linden flowers, mallow, peppermint, sage, thyme, wild thyme), glycerin, invert sugar (fructose/dextrose), natural flavor, starch syrup, sugar

Storage

Other Information Store in a dry place

Label version 6, effective 10 December 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

12 other listings state exactly the same active ingredient at exactly the same strength in the same dosage form, across 2 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 63667-503
• DailyMed label, set id 0baf383c-886d-47ca-8a6d-221298c79446
• How Lozenges builds these pages