NDC 72988-0012 Yobisin

Rehmannia Root, Angelica Gigas Root

NDC Product Code 72988-0012

NDC Code: 72988-0012

Proprietary Name: Yobisin 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: Rehmannia Root, Angelica Gigas 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

Color(s):
BROWN (C48332)
Shape: ROUND (C48348)
Size(s):
10 MM
Imprint(s):
T;2
Score: 1

NDC Code Structure

  • 72988 - Lydia Co., Ltd.
    • 72988-0012 - Yobisin

NDC 72988-0012-1

Package Description: 20 TABLET in 1 PACKAGE

NDC Product Information

Yobisin with NDC 72988-0012 is a a human over the counter drug product labeled by Lydia Co., Ltd.. The generic name of Yobisin is rehmannia root, angelica gigas root. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Lydia Co., Ltd.

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Yobisin 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.

  • RHUBARB 16.7 mg/1
  • REHMANNIA GLUTINOSA ROOT 416.7 mg/1
  • ANGELICA GIGAS ROOT 416.7 mg/1
  • AKEBIA STEM 416.7 mg/1
  • SCUTELLARIA BAICALENSIS ROOT 250 mg/1
  • LICORICE 125 mg/1
  • ALISMA PLANTAGO-AQUATICA ROOT 250 mg/1
  • FORSYTHIA SUSPENSA FRUIT 16.7 mg/1
  • PLANTAGO SEED 250 mg/1
  • GINGER 16.7 mg/1
  • CHINESE CINNAMON 16.7 mg/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.

  • MAGNESIUM STEARATE (UNII: 70097M6I30)

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.

Yobisin Product Label Images

Yobisin 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

Rehmannia root, angelica gigas root, akebia stem, scutellaria root, alisma rhizome, plantago seed, licorice, gardenia fruit, gentian root and rhizome, cinnamomum cassia presl, raw ginger, rhubarb, ephdra heab, forsythia fruit

Inactive Ingredient

Magnesium stearate, corn starch, polyethylene glycol 6000, hypromellose 2910

Otc - Purpose

Bladder qatar, urethritis, kidney disease, nephrotic syndrome, edema

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Adults: 3~6 tablets twice a day7 to 14 years old: 2-3 tablets twice a day

Warnings

Do not take this medicine if you have following symptomschildren under 6 years oldwomen who are likely to be pregnant or pregnantbreastfeeding

Dosage & Administration

For oral use only

* Please review the disclaimer below.

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