Label: BAEKCHO-DS- licorice ext syrup

  • NDC Code(s): 73442-0007-1
  • Packager: I World Pharmaceutical Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 13, 2024

If you are a consumer or patient please visit this version.

  • 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

    label

  • INGREDIENTS AND APPEARANCE
    BAEKCHO-DS 
    licorice ext syrup
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73442-0007
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE10 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73442-0007-1100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product03/29/201912/11/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/23/201912/11/2024
    Labeler - I World Pharmaceutical Co., Ltd. (688222857)
    Registrant - I World Pharmaceutical Co., Ltd. (688222857)
    Establishment
    NameAddressID/FEIBusiness Operations
    I World Pharmaceutical Co., Ltd.688222857manufacture(73442-0007)