FDA.reportPublic FDA data

Menthol Drops Dollar General Severe 45ct

Manufacturer
Dollar General Corporation
Effective date
2025-10-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:40:35

Label at a glance#

ProductMenthol Drops Dollar General Severe 45ct
Active ingredientLEVOMENTHOL
Label structure7 sections

Indications and uses

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

Dosage and administration

 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

Label contents#

Full prescribing information#

Active ingredient 

OTC - ACTIVE INGREDIENT SECTION

Menthol 20 mg

Purpose

OTC - PURPOSE SECTION

Oral anesthetic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical gelp or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

 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

Other information

SPL UNCLASSIFIED SECTION

  • 11 calories per drop
  • do not use if bags is torn or open
  • Contains: Soy

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75712-040-01Menthol Drops Dollar General Severe 45ct9 in 1 CARTONLOZENGE92
75712-040-01Menthol Drops Dollar General Severe 45ct45 in 1 BAGLOZENGE452

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75712-04075712-040-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
CORN SYRUP9G5L16BK6NIACT
EUCALYPTOLRV6J6604TKIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C RED NO. 40WZB9127XOAIACT
ACACIA5C5403N26OIACT
MALTODEXTRIN7CVR7L4A2DIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
LEVOMENTHOLBZ1R15MTK7ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-03-12full-release2026-06-01 00:09:52

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Menthol Drops Dollar General Severe 45ctMENTHOLDollar General Corporationc831d3d9-b910-40e6-bfdf-defe6850614d2025-10-24WarningsExact identifier
ndc (package): 75712-040-01
ndc (product): 75712-040
ndc11 (package): 75712004001
spl id: 41eb6ee3-ec97-283a-e063-6294a90ad49c
spl set id: c831d3d9-b910-40e6-bfdf-defe6850614d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.