CVS Menthol Medicated Throat Drops

Manufacturer
CVS Pharmacy | Bestco Inc.
Effective date
2019-04-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:10

Label at a glance#

ProductCVS Menthol Medicated Throat Drops
Active ingredientMENTHOL
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each drop)

Menthol 20 mg

OTC - PURPOSE SECTION

Purpose

Oral anesthetic

INDICATIONS & USAGE SECTION

Uses temporarily relieves:

  • occasional minor irritation and pain associated with sore throat and sore mouth

WARNINGS SECTION

Warnings

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • a severe sore throat accompanied by difficulty in breathing or that lasts more than 2 days.
  • a sore throat accompanied by fever, headache, rash, swelling, nausea or vomiting.

OTC - STOP USE SECTION

Stop use and consult doctor if

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - WHEN USING SECTION

Do not exceed recommended dosage.

DOSAGE & ADMINISTRATION SECTION

DIrections

adults and children 12 years and over - dissolve 1 drop slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.

children 12 years and under - do not use

OTHER SAFETY INFORMATION

Other information

  • 10 calories per drop
  • do not use if bag is torn or open

INACTIVE INGREDIENT SECTION

Inactive ingredients: Corn starch, corn syrup, eucalyptus oil, FD&C blue no. 1, glycerin, gum arabic, medium chain triglycerides, potassium sorbate, soybean oil, sucrose and water.

OTC - QUESTIONS SECTION

Questions? Or to report an adverse event call 1-800-245-2898. Monday - Friday, 9AM to 4PM EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS Menthol Medicated Drop 45ctCVS Menthol Medicated Drop 45ct

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1995300menthol 20 MG Oral LozengePSN1
1995300menthol 20 MG Oral LozengeSCD1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69842-356-452021-01-29C16284748780-1ba0f9c33-3a62-a910-e053-dadaa90a0b85Menthol 20 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-356-45CVS Menthol Medicated Throat Drops45 in 1 BAGLOZENGE451

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-356CVS MENTHOL MEDICATED THROAT DROPS (MENTHOL) LOZENGE [CVS PHARMACY]1Legacy NDC, 1 package rows20190412_86465a67-9044-ed8f-e053-2991aa0ad4eb.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-35669842-356-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

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
86465a67-9045-ed8f-e053-2991aa0ad4eb86465a67-9044-ed8f-e053-2991aa0ad4eb2019-04-11WarningsExact identifier
spl id: 86465a67-9045-ed8f-e053-2991aa0ad4eb
spl set id: 86465a67-9044-ed8f-e053-2991aa0ad4eb

Reported adverse events (FAERS/openFDA)#

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