Menthol Cough Drops Honey Lemon Flavor

Manufacturer
CVS Pharmacy | Boston Nutraceutical Science SL | Boston Nutraceutical Production SL
Effective date
2025-09-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:13:39

Label at a glance#

ProductMenthol Cough Drops Honey Lemon Flavor
Active ingredientMENTHOL
Label structure15 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

  • Menthol 7.5 mg.............cough suppresant/ oral anesthetic

OTC - PURPOSE SECTION

Uses temporarily relieves:

  • cough as may occur with a cold
  • ocassional minor irritation and sore throat

INDICATIONS & USAGE SECTION

Uses temporarily relieves:

cough as may occur with a cold

ocassional minor irritation and sore throat

WARNINGS SECTION

Warnings

Sore throat warning: severe or persistence sore throat accompanied by high fever, headache, nausea and vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days.

OTC - ASK DOCTOR SECTION

Stop and consult a doctor before use if

  • cough persist 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 mouth symptoms do not improve in 7 days, or if irritation, pain or redness persists or worsens.

OTC - STOP USE SECTION

Stop and consult a doctor before use if

  • cough persist 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 mouth symptoms do not improve in 7 days, or if 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 this and all drugs out of the reach of children.

OVERDOSAGE SECTION

In case of accidental overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Adults and children 6 years and over: dissolve 1 drop slowly in the mouth. Repeated every 2 hours as needed or as directed by a doctor.
  • Children under 6 years: as a doctor

OTHER SAFETY INFORMATION

  • 10 calories per drop
  • Store in a cool and dry place

INACTIVE INGREDIENT SECTION

citric acid, glucose syrup, honey, natural flavors, sucrose, turmeric (for coloring)

Back labelBack label

OTC - QUESTIONS SECTION

Questions? or to report and adverse event call: 1-833-552-1767

RECENT MAJOR CHANGES SECTION

  • Directions
  • Stop and consult a doctor
  • Warning

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1250189menthol 7.5 MG Oral LozengePSN1
1250189menthol 7.5 MG Oral LozengeSCD1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-987-01Menthol Cough Drops Honey Lemon Flavor140 in 1 BAGPASTILLE1401

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
51316-98751316-987-01

Ingredients#

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

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

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
Menthol Cough Drops Honey Lemon FlavorMENTHOL HONEY LEMON FLAVORCVS Pharmacy3eab4cf9-6fdc-a6fb-e063-6394a90a86332025-09-13WarningsExact identifier
ndc (package): 51316-987-01
ndc (product): 51316-987
ndc11 (package): 51316098701
spl id: 3eab4d2c-df74-97cf-e063-6394a90a5ee0
spl set id: 3eab4cf9-6fdc-a6fb-e063-6394a90a8633

Reported adverse events (FAERS/openFDA)#

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