Halls Sugar Free Mountain Menthol

The listing

NDC product code

12546-640 (labeller 12546, product 640)

Labeller

Mondelez Global LLC

Brand name

Halls Sugar Free Mountain Menthol

Generic name

Menthol

Dosage form

Lozenge

Route

oral

Marketing category

OTC MONOGRAPH DRUG M012

Marketing start

3 June 2019

Listing expires

31 December 2026

RxNorm concept

476973

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

<(per drop) Menthol 5.8 mg>

Purpose

<Cough Suppressant, Oral Anesthetic>

Uses

<temporarily relieves: cough due to a cold occasional minor irritation or sore throat>

Warnings

<Sore throat warnings: if sore throat is severe, persist for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These may be serious.>

Ask a doctor before use

persistent or 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. sore mouth does not improve in 7 days irritation, pain, or redness persists or worsens

Keep out of reach of children

Keep out of reach of children. Enter section text here

Directions

adults and children 5 years and over: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed. children under 5 years: ask a doctor

Inactive ingredients

<acesulfame potassium, aspartame, eucalyptus oil, FDC Blue 1, FDC Red 40, flavors, isomalt, sodium carboxymethylcellulose, soy lecithin, water>

Other information

<Call 1-800-524-2854 , Monday to Friday, 9 AM - 6 PM Eastern Time or visit our website at www.gethalls.com>

Label version 8, effective 15 August 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

66 other listings state exactly the same active ingredient at exactly the same strength in the same dosage form, across 37 different labellers. They are not necessarily the same product: inactive ingredients, flavour and pack size differ, and this site does not compare prices.

Showing the first 40 of 66. The rest are reachable from each ingredient page.

Sources for this page

• FDA National Drug Code Directory entry for 12546-640
• DailyMed label, set id 54e0d57e-1f48-45e2-86b3-0e50775996f4
• How Lozenges builds these pages