Baekcho-DS

Manufacturer
Lydia Co., Ltd. | Green Cross Corp_Eumseong Plant
Effective date
2019-04-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:28:23

Label at a glance#

ProductBaekcho-DS
Active ingredientLICORICE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Licorice Ext

INACTIVE INGREDIENT SECTION

Glycerine,menthol oil,sucralose,xylitol,purified water,etc

OTC - PURPOSE SECTION

(Loss of appetite), stomach bloating, dyspepsia, overeating, nausea, vomiting, suicide, constipation, dilute stools,

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Adult and 15 years and older: 1 time 10 mL
Pediatric patients were divided into two groups: 1 to 11 years old, 6.5 mL, 8 to 10 years old, 5.0 mL, 5 to 7 years old, 3.5 mL, 3-4 years old, 2.5 mL,
Take it three times a day after meals. The interval should be 4 hours or more.

WARNINGS SECTION

1. Do not take this medicine.
Do not take to infants (infants, babies) under 3 months. In addition, infants (infants and young babies) who are under the age of one for at least three months must give priority to receiving medical attention, and should not be taken unless they are inevitable.

2. Consult a doctor, dentist or pharmacist before taking this medicine.
1) patients with hypertension, elderly (elderly), cardiac or renal (kidney) patients, edema (swelling) patients
2) People who are taking other medicines: potassium-containing preparations, licorice-containing preparations, glycyrrhizic acid or its salt-containing preparations, loop-type diuretics (furosemide, ethacrynic acid) or thiazide diuretics (trichloromethiazide) (Combined with) Aldosteronism or hypokalemia due to myocarditis (myopathy) is likely to occur due to taking it carefully.
3) Patients receiving medical treatment

3. Immediately stop taking this drug and consult a doctor, dentist or pharmacist if: Have this attached document at the time of consultation.
1) Upper aldosteronism: If you have decreased urine volume, face and hands and feet are swollen, your eyelids are getting heavy, your hands are hardening, your blood pressure is getting high or you have a headache (such as a maximum dose of 1g per day as a licorice, Observation (measurement of serum potassium levels) should be sufficient and should be discontinued if abnormality is confirmed, because gastric aldosteronism such as elevation of blood pressure, elevation of blood pressure, retention of sodium body fluid (swelling), swelling (swelling)
2) Myopathy (myopathy): As a result of hypokalemia, myopathy (myopathy) may occur. If the observation is sufficient and anomalies such as helplessness, cramps and paralysis are confirmed
3) If there is no improvement in symptoms even for several days

4. Other cautions when taking this medicine
1) Keep the prescribed dosage and dosage.
2) When taking a child, take it under the supervision of a guardian.
3) Do not take it for a long time.

5. Storage Precautions
1) Keep out of reach of children.
2) Taking medicines out of their original containers and storing them in other containers may cause accidents or poor quality of medicines due to misuse (misuse), so keep them in their original container and keep them tightly closed.
3) Avoid direct sunlight and store in a cool, dry place.

DOSAGE & ADMINISTRATION SECTION

for oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72988-0009-12025-11-20C16284748780-1ba0f9c33-57ea-a910-e053-dadaa90a0b85Drug Facts
72988-0009-12021-01-29C16284748780-1ba0f9c33-57ea-a910-e053-dadaa90a0b85Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72988-0009BAEKCHO-DS (LICORICE EXT) SYRUP [LYDIA CO., LTD.]1Legacy NDC20190403_859906f4-7ad9-e41f-e053-2a91aa0ab1b8.zip

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
72988-000972988-0009-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
LICORICE61ZBX54883ACTIB
GLYCERINPDC6A3C0OXIACT
SUCRALOSE96K6UQ3ZD4IACT
MENTHOLL7T10EIP3AIACT

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
44014fd2-c912-83d5-e063-6394a90a008a859906f4-7ad9-e41f-e053-2a91aa0ab1b82025-11-20WarningsExact identifier
spl set id: 859906f4-7ad9-e41f-e053-2a91aa0ab1b8

Reported adverse events (FAERS/openFDA)#

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