NDC 72988-0011 Baenosin

Platycodon Root, Licorice, Jujube, Peony Root

NDC Product Code 72988-0011

NDC Code: 72988-0011

Proprietary Name: Baenosin What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Platycodon Root, Licorice, Jujube, Peony Root What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

BLUE (C48333)
Shape: OVAL (C48345)
25 MM
Score: 1

NDC Code Structure

  • 72988 - Lydia Co., Ltd.
    • 72988-0011 - Baenosin

NDC 72988-0011-1

Package Description: 10 CAPSULE in 1 PACKAGE

NDC Product Information

Baenosin with NDC 72988-0011 is a a human over the counter drug product labeled by Lydia Co., Ltd.. The generic name of Baenosin is platycodon root, licorice, jujube, peony root. The product's dosage form is capsule and is administered via oral form.

Labeler Name: Lydia Co., Ltd.

Dosage Form: Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.

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.

Baenosin 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 .5 g/1
  • JUJUBE FRUIT .5 g/1
  • GINGER .5 g/1

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.


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: 04-22-2019 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.

Baenosin Product Label Images

Baenosin 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

Platycodon root, licorice, jujube, peony root, ginger, poncirus immature fruit

Inactive Ingredient

Lactose monohydrate, acacia, corn starch, carboxymethylcellulose calcium, l-menthol

Otc - Purpose

Pyrogenic diseases with redness, swelling, stiffness and pain

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Adults take 2 capsules 3 times a day before meals or between meals


Do not take this medicine if you have following symptomssymptoms of headaches, chills, and fever other than local symptoms such as spasm (red with blood), swelling, and pain at the same time

Dosage & Administration

For oral use only

* Please review the disclaimer below.

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