HyVee Cough Drops Menthol

Manufacturer
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | Medical Group Care LLC
Effective date
2026-01-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:31:00

Label at a glance#

ProductHyVee Cough Drops Menthol
Active ingredientMENTHOL
Label structure12 sections

Dosage and administration

■ adults and children 2 years and over: dissolve lozenge slowly in the mouth. Repeat every 2 hours as needed or directed by doctor. ■ children under 2 years: ask a doctor.

Storage and handling

■ store at room temperature ■ Keep away from excessive heat or sunlight ■ do not use if primary bag seal has been torn or broken ■ contains: SOY.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Menthol 5.4 mg

Purpose

OTC - PURPOSE SECTION

Purposes cough suppressant, oral anesthetic

Use

INDICATIONS & USAGE SECTION

temporary relieves: ■ cough due to cold ■ occasional minor irritation or sore throat

Warnings

WARNINGS SECTION

Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or follow headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. 

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 accompained by fever, rash, or persistent headache. These could be signs of a serius 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 this and all drugs out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

■ adults and children 2 years and over: dissolve lozenge slowly in the mouth. Repeat every 2 hours as needed or directed by doctor.

■ children under 2 years: ask a doctor.

Other information

STORAGE AND HANDLING SECTION

■ store at room temperature ■ Keep away from excessive heat or sunlight ■ do not use if primary bag seal has been torn or broken ■ contains: SOY.

Inactive ingredients

INACTIVE INGREDIENT SECTION

citric acid, corn syrup, eucalyptus oil, gardenian blue, menthol flavor, potassium citrate, soy lecithin, sucralose, sucrose, water

OTC - QUESTIONS SECTION

Call +1-866-306-9136

You may also report concerns to this phone number

Monday to Friday, 9 AM - 5 PM Eastern Time or visit our website at www.mgc.us

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
485287menthol 5.4 MG Oral LozengePSN2
485287menthol 5.4 MG Oral LozengeSCD2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83698-901-30HyVee Cough Drops Menthol30 in 1 BAGLOZENGE302

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83698-90183698-901-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
HyVee Cough Drops MentholMENTHOLXiamen Kang Zhongyuan Biotechnology Co., Ltd.8cac1229-8e8e-4d8c-9f18-c2cd0f6f50bd2026-01-02WarningsExact identifier
ndc (package): 83698-901-30
ndc (product): 83698-901
ndc11 (package): 83698090130
spl id: 476950e2-0c8a-c623-e063-6294a90a343f
spl set id: 8cac1229-8e8e-4d8c-9f18-c2cd0f6f50bd

Reported adverse events (FAERS/openFDA)#

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