Unishield Cherry Cough Drops

Manufacturer
Unishield | Unifirst First Aid Corporation
Effective date
2025-09-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:13:18

Label at a glance#

ProductUnishield Cherry Cough
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure14 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each drop)

Menthol 7.6 mg

OTC - PURPOSE SECTION

Purpose

Antitussive (cough suppressant)/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

  • 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 older)

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 59º-86ºF (15º-30ºC)
  • protect from moisture & heat

INACTIVE INGREDIENT SECTION

Inactive ingredients:

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

OTC - PURPOSE SECTION

Questions or comments? 800-480-5855

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unishield

Cough Drop

Cough Suppressant/Oral Anesthetic

50 Drops/Individually Wrapped

Cherry Flavored

Menthol 7.6 mg

Pull To Open

• Temporarily relieves sore throat and cough

• Pleasant tasting formula

• Menthol vapors ease congestion

Compare active ingredients to:

Hall®

Registered Trademark of Warner-Lambert

Individually Wrapped Cough Drops

050R050R

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
359751menthol 7.6 MG Oral LozengePSN5
359751menthol 7.6 MG Oral LozengeSCD5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49314-0505-5Unishield Cherry Cough50 in 1 BOXLOZENGE505

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49314-050549314-0505-5

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
Unishield Cherry CoughMENTHOLUnishieldb8297bc1-44b2-3de0-e053-2995a90ad01b2025-09-09WarningsExact identifier
ndc (package): 49314-0505-5
ndc (product): 49314-0505
ndc11 (package): 49314050505
spl id: 3e5d6186-80a9-5eb7-e063-6294a90a235f
spl set id: b8297bc1-44b2-3de0-e053-2995a90ad01b

Reported adverse events (FAERS/openFDA)#

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