BAEKCHO-DS- licorice ext syrup

Baekcho-DS by

Drug Labeling and Warnings

Baekcho-DS by is a Otc medication manufactured, distributed, or labeled by I World Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Licorice Ext

INACTIVE INGREDIENT

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

PURPOSE

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

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

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

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

for oral use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BAEKCHO-DS 
licorice ext syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73442-0007
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883)	LICORICE	10 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SUCRALOSE (UNII: 96K6UQ3ZD4)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73442-0007-1	100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	03/29/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/23/2019

Labeler - I World Pharmaceutical Co., Ltd. (688222857)

Registrant - I World Pharmaceutical Co., Ltd. (688222857)

Establishment
Name	Address	ID/FEI	Business Operations
I World Pharmaceutical Co., Ltd.		688222857	manufacture(73442-0007)