HanPoong Beat Cold

Manufacturer
HANPOONG PHARM CO.,LTD.
Effective date
2021-11-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:19:50

Label at a glance#

ProductHanPoong Beat Cold
Active ingredientEPHEDRINE HYDROCHLORIDE
Label structure17 sections

Storage and handling

Other Information ■ store in a cool, dry place between 1℃~30℃(33.8℉~86℉)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ephedrine HCl 5.34 mg

OTC - PURPOSE SECTION

Bronchodilator

OTC - WHEN USING SECTION

for temporary relief of mild symptoms of intermittent asthma: ■ wheezing ■ tightness of chest ■ shortness of breath

WARNINGS SECTION

Asthma alert: Because asthma may be life threatening, see a doctor if you
■ are not better in 60 minutes ■ get worse
■ need more than 28 sachets in 24 hours
■ use more than 18 sachets in 24 hours for 3 or more days a week ■ have more than 2 asthma attacks in a week
■ These may be signs that your asthma is getting worse. ■ This product will not give you asthma relief as quickly as an inhaled bronchodilator.

OTC - DO NOT USE SECTION

■ unless a doctor said you have asthma
■ if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs taken for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

OTC - ASK DOCTOR SECTION

■ ever been hospitalized for asthma ■ heart disease
■ high blood pressure ■ diabetes ■ thyroid disease ■ seizures ■ narrow angle glaucoma ■ a psychiatric or emotional condition ■ trouble urinating due to an enlarged prostate gland

OTC - ASK DOCTOR/PHARMACIST SECTION

■ taking prescription drugs for asthma, obesity, weight control, depression, or psychiatric or emotional conditions
■ taking any drug that contains phenylephrine, pseudoephedrine, ephedrine, or caffeine (such as for allergy, cough-cold, or pain)

OTC - WHEN USING SECTION

When using this product
■ your blood pressure or heart rate may go up. This could increase your risk of heart attack or stroke, which may cause death.
■ your risk of heart attack or stroke increases if you: ● have a history of high blood pressure or heart disease ● take this product more frequently or take more than the recommended dose ■ avoid foods or beverages that contain caffeine
■ avoid dietary supplements containing ingredients reported or claimed to have a stimulant effect

OTC - STOP USE SECTION

Stop use and ask a doctor if ■ your asthma is getting worse (see Asthma alert) ■ you have difficulty sleeping ■ you have a rapid heart beat ■ you have tremors, nervousness, or seizure

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

INDICATIONS & USAGE SECTION

Directions
■ Do not take more than directed

DOSAGE & ADMINISTRATION SECTION

■ adults and children 12 years of age and over: oral dose is 12.5 to 25 milligrams every 4 hours as needed. Do not take more than 150 milligrams in 24 hours
■ children under 12 years of age: ask a doctor

STORAGE AND HANDLING SECTION

Other Information
■ store in a cool, dry place between 1℃~30℃(33.8℉~86℉)

INACTIVE INGREDIENT SECTION

Croscarmellose sodium, Herbal extract (Cinnamomum cassia, Ephedra, Ginger, Jujube, Kudzu, Licorice, Paeonia lactiflora root), Hypromellose, Magnesium stearate, Microcrystalline cellulose, Polyethylene glycol 6000, Silicon dioxide, Titanium oxide,
FD&C Blue No. 1, FD&C Red No. 40, Food Yellow No.5 Aluminium Lake

OTC - QUESTIONS SECTION

Questions or comments? +1-800-829-4933

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product out boxProduct out boxProduct sachetProduct sachet

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82369-111182369-1111-2, 82369-1111-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
f0dee721-4da1-0a15-e053-2a95a90adf65d07b3324-c87c-bb7a-e053-2a95a90a3d512022-12-28WarningsExact identifier
spl set id: d07b3324-c87c-bb7a-e053-2a95a90a3d51

Reported adverse events (FAERS/openFDA)#

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