Severe Throat Sore Drops

The listing

NDC product code

11673-143 (labeller 11673, product 143)

Labeller

Target Corporation Inc.

Brand name

Severe Throat Sore Drops

Generic name

Menthol

Dosage form

Pastille

Route

oral

Marketing category

OTC MONOGRAPH DRUG M012

Marketing start

12 October 2019

Listing expires

31 December 2026

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 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 20mg Cough Suppressant Oral anesthetic

Purpose

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

Uses

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

Warnings

Sore throat warning: severe or persistence sore throat accompanied or followed 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

eucalyptus oil, FD&C Blue No.1, glucose syrup, gum arabic, sucrose Back Label

Other information

or to report and adverse event call: 1-617-848-4560 Monday to Friday 9AM to 4 PM east

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.

Sources for this page

• FDA National Drug Code Directory entry for 11673-143
• DailyMed label, set id 949543d5-5043-ac06-e053-2995a90ab398
• How Lozenges builds these pages