McKesson Cough Supressant

Manufacturer
McKesson Medical-Surgical | Unifirst First Aid Corporation
Effective date
2025-09-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:13:20

Label at a glance#

ProductMcKesson Cough Supressant
Active ingredientMENTHOL
Label structure14 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Menthol 7.6 mg

OTC - PURPOSE SECTION

Purpose

Antitussive (cough supressant)/oral anesthetic

INDICATIONS & USAGE SECTION

Uses

Temporarily relieves

■ cough as may occur with a cold or inhaled irritants

■ 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, nausea, or vomiting, consult a doctor promptly. These symptoms may be serious.

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 - 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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • do not use more than directed

​

Adults and children:
(12 years and over)

Allow 1 drop to dissolve slowly in the mouth. May be repeated every 2 hours as necessary or as directed by a doctor.

Children under 12 years:

Ask a doctor

OTHER SAFETY INFORMATION

Other information

  • 15 calories per drop
  • store at 59-86°F (15°-30°C)
  • protect from moisture & heat

INACTIVE INGREDIENT SECTION

Inactive ingredients

cherry flavor, corn syrup, eucalyptus oil, FD&C red #40, sucrose

OTC - QUESTIONS SECTION

Questions or comments? Call 1-800-777-4908

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 68599-0500-3

McKesson

Cough Suppressant

Oral Anesthetic Drops

Cherry Flavored

Each Lozenge Contains Menthol 7.6 mg

For temporary cough relief due to minor throat and bronchial irritation as may occur with a cold or inhaled irritants.

300

Lozenges Per Box

MFR # 98008

050R050R

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
359751menthol 7.6 MG Oral LozengePSN3
359751menthol 7.6 MG Oral LozengeSCD3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68599-0500-3McKesson Cough Supressant300 in 1 CARTONLOZENGE3003

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68599-050068599-0500-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
McKesson Cough SupressantMENTHOLMcKesson Medical-Surgicaldb5e0490-2ed8-2d53-e053-2a95a90a98f52025-09-09WarningsExact identifier
ndc (package): 68599-0500-3
ndc (product): 68599-0500
ndc11 (package): 68599050003
spl id: 3e5d77e9-9140-41d7-e063-6294a90a365e
spl set id: db5e0490-2ed8-2d53-e053-2a95a90a98f5

Reported adverse events (FAERS/openFDA)#

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