Menthol Drops Dollar General Severe 45ct

The listing

NDC product code

75712-040 (labeller 75712, product 040)

Labeller

Dollar General Corporation

Brand name

Menthol Drops Dollar General Severe 45ct

Generic name

MENTHOL

Dosage form

Lozenge

Route

oral

Marketing category

OTC MONOGRAPH DRUG M012

Marketing start

15 March 2024

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 purposeOral 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

Menthol 20 mg Purpose Oral anesthetic

Purpose

Oral anesthetic

Uses

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

Warnings

Sore throat warning: ore throat warning: severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 12 years of age. Ask a doctor before use if you have: a severe sore throat accompanied by difficult in breathing or that lasts more than 2 days a sore accompanied by fever, headache, rash, swelling, nausea or vomiting Stop use and ask a doctor if sore mouth symptoms do not improve in 7 days, or if irritation, pain or redness lasts or worsens If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children. In case of overdose, get medical gelp or contact a Poison Control Center right away

Keep out of reach of children

Keep out of reach of children. In case of overdose, get medical gelp or contact a Poison Control Center right away

Directions

adults and children 12 years and over dissolve 1 lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor. children under 12 years do not use

Inactive ingredients

Corn Syrup; eucalytus oil; FD&C blue no. 1; FD&C red no. 40; Gum Arabic; Maltodextrin; natural flavor; soy lecithin; sucrose and water

Label version 2, effective 24 October 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

One other listing states exactly the same active ingredient at exactly the same strength in the same dosage form. 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 75712-040
• DailyMed label, set id c831d3d9-b910-40e6-bfdf-defe6850614d
• How Lozenges builds these pages