cherry cough drops

Manufacturer
CVS Pharmacy | BestCo Inc.
Effective date
2019-12-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:01:50

Label at a glance#

Productcherry cough drops
Active ingredientMENTHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each drop)

Menthol 5.8 mg

OTC - PURPOSE SECTION

Cough suppressant/Oral anesthetic

INDICATIONS & USAGE SECTION

Uses temporarily relieves:

cough as may occur with a cold

occasional minor irritation and sore throat

WARNINGS SECTION

Warnings

Sore throat warning: 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. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

persistant or chronic cough such as occurs with smoking, asthma, or emphysema

cough accompanied by excessive phlegm (mucus)

OTC - STOP USE SECTION

Stop use and consult doctor if

cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistant headache. These could be signs of a serious condition.

sore throat is severe, or irritation, pain or redness lasts or worsens

sore mouth does not improve in 7 days

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.

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 5 years of age and over: allow 1 drop to dissolve slowly in mouth. May be repeated every two hours as necessary or as directed by a doctor.

Children under 5 years of age: ask a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients: Corn starch, corn syrup, eucalyptus oil, FD&C red #40, glycerin, medium chain triglycerides, natural and artificial flavors, 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 Cherry 30ct 501998CVS Cherry 30ct 501998

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
476973menthol 5.8 MG Oral LozengePSN2
476973menthol 5.8 MG Oral LozengeSCD2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59779-655-302022-01-28C16284748780-1d6a99b39-36a1-a426-e053-dadaa90af4c2Menthol 5.8mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59779-655-30cherry cough drops30 in 1 BAGLOZENGE302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-655CHERRY COUGH DROPS (MENTHOL) LOZENGE [CVS PHARMACY]2Legacy NDC, 1 package rows20191210_2db57bff-e3fb-6fc4-e054-00144ff88e88.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
59779-65559779-655-30

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
994a8595-a2a7-14d8-e053-2995a90aa4472db57bff-e3fb-6fc4-e054-00144ff88e882019-12-09WarningsExact identifier
spl id: 994a8595-a2a7-14d8-e053-2995a90aa447
spl set id: 2db57bff-e3fb-6fc4-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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