Menthol Cough Drops

Manufacturer
Target Corporation Inc. | Boston Nutraceutical Science SL | Boston Nutraceutical Production SL
Effective date
2024-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:12:31

Label at a glance#

ProductMenthol Cough Drops
Active ingredientMENTHOL
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient 5.8 mg

Cough Suppressant

Oral anesthetic

Front PanelFront Panel

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

Ask a doctor before use if you have

  • persistent or chronic cough such as occurs with smoking, asthma or emphysema
  • cough accompany by excessive phem (mucus)

OTC - STOP USE SECTION

Stop use and consult a doctor if

  • cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash or persisten headache. These could be signs of a serious condition
  • sore mouth symptons 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 mouth. Repeated every 2 hours as needed or as directed by a doctor.
  • Children under 6 years ask a doctor

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT SECTION

blackcurrant and black carrot extract (coloring), citric acid, flavors, glucose syrup, sucrose

Back PanelBack Panel

OTC - QUESTIONS SECTION

Questions? or to report and adverse event call: 1-800-910-6874

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BackBack

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
476973menthol 5.8 MG Oral LozengePSN1
476973menthol 5.8 MG Oral LozengeSCD1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-200-01Menthol Cough Drops80 in 1 BAGPASTILLE801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82442-200MENTHOL COUGH DROPS (MENTHOL) PASTILLE [TARGET CORPORATION INC.]1Current NDC, 1 package rows20240516_187622dc-ecde-181d-e063-6294a90a4e8f.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-20082442-200-01

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 DropsMENTHOLTarget Corporation Inc.187622dc-ecde-181d-e063-6294a90a4e8f2024-05-14WarningsExact identifier
ndc (package): 82442-200-01
ndc (product): 82442-200
ndc11 (package): 82442020001
spl id: 18763ea4-7755-e740-e063-6394a90a4351
spl set id: 187622dc-ecde-181d-e063-6294a90a4e8f

Reported adverse events (FAERS/openFDA)#

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