Cherry Cough Drops

Manufacturer
Meijer | BestCo Inc.
Effective date
2018-11-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:57:08

Label at a glance#

ProductCherry Cough Drops
Active ingredientMENTHOL
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each drop)

Menthol 5.8mg

OTC - PURPOSE SECTION

Purpose

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, persists 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:

  • perisistent or chronic cough such as occurs with

smoking, asthma, or emphysema

  • cough accompanied by excessive phlegm (mucus)

OTC - STOP USE SECTION

Stop use and ask doctor if

  • cough persists for more than 7 days, tends to recur, or

is accompanied by fever, rash, or persistent 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 and over dissolve 1 lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.

children under 5 years ask a doctor

OTHER SAFETY INFORMATION

Other Information 10 calories per drop

INACTIVE INGREDIENT SECTION

Inactive ingredients: Corn starch, corn syrup,

eucalyptus oil, FD&C red no 40, glycerin, medium chain

triglycerides, natual & artificial flavors, soybean oil,

sucrose and water.

OTC - QUESTIONS SECTION

Question? Call (888) 309-9030.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Meijer Cherry 30ctMeijer Cherry 30ct

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
41250-113-302020-01-31C16284748780-19d75b9d0-38d4-f424-e053-dadaa90a57ceMenthol 5.8 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-113-30Cherry Cough Drops30 in 1 BAGLOZENGE302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-113CHERRY COUGH DROPS (MENTHOL) LOZENGE [MEIJER]2Legacy NDC, 1 package rows20181102_3c052e93-55a5-16ce-e054-00144ff8d46c.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
41250-11341250-113-30

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
WATER059QF0KO0RIACT
MENTHOLL7T10EIP3AACTIB

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
799e8fd0-596a-7e61-e053-2991aa0a2be53c052e93-55a5-16ce-e054-00144ff8d46c2018-11-01WarningsExact identifier
spl id: 799e8fd0-596a-7e61-e053-2991aa0a2be5
spl set id: 3c052e93-55a5-16ce-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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