NDC 72988-0009 Baekcho-ds

Licorice Ext

NDC Product Code 72988-0009

NDC Product Information

Baekcho-ds with NDC 72988-0009 is a a human over the counter drug product labeled by Lydia Co., Ltd.. The generic name of Baekcho-ds is licorice ext. The product's dosage form is syrup and is administered via oral form.

Labeler Name: Lydia Co., Ltd.

Dosage Form: Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Baekcho-ds Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • LICORICE 10 g/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • SUCRALOSE (UNII: 96K6UQ3ZD4)
  • MENTHOL (UNII: L7T10EIP3A)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Lydia Co., Ltd.
Labeler Code: 72988
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-23-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Baekcho-ds Product Label Images

Baekcho-ds Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Licorice Ext

Inactive Ingredient

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

Otc - Purpose

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

Otc - 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

* Please review the disclaimer below.

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