FDA.reportPublic FDA data

Xpect Cherry Cough Drops

Manufacturer
Cintas Corporation | Riclan S.A.
Effective date
2025-09-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:14:37

Label at a glance#

ProductXpect Cherry Cough Drops
Active ingredientMENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each drop)

Menthol 7 mg

OTC - PURPOSE SECTION

Purpose

Cough suppressant/oral anesthetic

INDICATIONS & USAGE SECTION

Uses

temporarily relieves:

  • cough due to a cold
  • occasional minor irritation or sore throat

WARNINGS SECTION

Warnings

Sore throat warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, rash, swelling, nausea, or vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days unless directed by a doctor. 

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • persistent 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 a doctor if 

  • cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. 
  • sore mouth does not improve in 7 days
  • irritation, pain, or redness persists or worsens

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

  • do not take more than directed 
  • adults and children 5 years and over: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed.
  • children under 5 years: ask a doctor

OTHER SAFETY INFORMATION

Other information

  • 12 calories per drop
  • Contains: SOY

INACTIVE INGREDIENT SECTION

Inactive ingredients 

corn syrup, eucalyptus oil, FD&C red #40, natural & artificial flavors, soy lecithin, sucrose, water

OTC - QUESTIONS SECTION

Questions or comments?

1-877-973-2811 Monday - Friday 8:00 am - 5:00 pm 

Principal Display Panel 42961-232-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CHERRY COUGH DROP

Menthol

Cough suppressant/oral anesthetic

  • Soothes sore throat
  • Temporarily relieves cough
  • Contains a menthol cough suppressant and oral anesthetic

Xpect® First aid

50 Individually Wrapped Drops

50Box50Box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
253015menthol 7 MG Oral LozengePSN3
253015menthol 7 MG Oral LozengeSCD3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42961-232-01Xpect Cherry Cough Drops1 in 1 PACKETLOZENGE13
42961-232-02Xpect Cherry Cough Drops50 in 1 BOXLOZENGE503
42961-232-03Xpect Cherry Cough Drops100 in 1 BOXLOZENGE1003

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42961-23242961-232-01, 42961-232-02, 42961-232-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
CORN SYRUP9G5L16BK6NIACT
EUCALYPTUS OIL2R04ONI662IACT
FD&C RED NO. 40WZB9127XOAIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
SUCROSEC151H8M554IACT
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
Xpect Cherry Cough DropsCHERRY COUGH DROPSCintas Corporationd1fd2f23-5435-405d-a7fd-644691f79e802025-09-23WarningsExact identifier
ndc (package): 42961-232-01
ndc (package): 42961-232-02
ndc (package): 42961-232-03
ndc (product): 42961-232
ndc11 (package): 42961023202
ndc11 (package): 42961023203
ndc11 (package): 42961023201
spl id: ecfc66a4-c8b7-4dfa-93ed-7b95307a6082
spl set id: d1fd2f23-5435-405d-a7fd-644691f79e80

Reported adverse events (FAERS/openFDA)#

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