NDC 72988-0012 Yobisin
Rehmannia Root,Angelica Gigas Root Tablet Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 72988-0012?
What are the uses for Yobisin?
What are Yobisin Active Ingredients?
- AKEBIA STEM 416.7 mg/1
- ALISMA PLANTAGO-AQUATICA ROOT 250 mg/1
- ANGELICA GIGAS ROOT 416.7 mg/1
- CHINESE CINNAMON 16.7 mg/1 - A plant species of the genus CINNAMOMUM that contains CINNAMATES and has been used in traditional Chinese medicine (DRUGS, CHINESE HERBAL).
- FORSYTHIA SUSPENSA FRUIT 16.7 mg/1
- GINGER 16.7 mg/1
- LICORICE 125 mg/1
- PLANTAGO SEED 250 mg/1 - Dried, ripe seeds of PLANTAGO PSYLLIUM; PLANTAGO INDICA; and PLANTAGO OVATA. Plantain seeds swell in water and are used as demulcents and bulk laxatives.
- REHMANNIA GLUTINOSA ROOT 416.7 mg/1
- RHUBARB 16.7 mg/1
- SCUTELLARIA BAICALENSIS ROOT 250 mg/1
Which are Yobisin UNII Codes?
The UNII codes for the active ingredients in this product are:
- RHUBARB (UNII: G280W4MW6E)
- RHUBARB (UNII: G280W4MW6E) (Active Moiety)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) (Active Moiety)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX) (Active Moiety)
- AKEBIA STEM (UNII: 531B9G152H)
- AKEBIA STEM (UNII: 531B9G152H) (Active Moiety)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (Active Moiety)
- LICORICE (UNII: 61ZBX54883)
- LICORICE (UNII: 61ZBX54883) (Active Moiety)
- ALISMA PLANTAGO-AQUATICA ROOT (UNII: 6DXR2088WL)
- ALISMA PLANTAGO-AQUATICA ROOT (UNII: 6DXR2088WL) (Active Moiety)
- FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5)
- FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5) (Active Moiety)
- PLANTAGO SEED (UNII: 9C60Y73166)
- PLANTAGO SEED (UNII: 9C60Y73166) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- CHINESE CINNAMON (UNII: WS4CQ062KM) (Active Moiety)
Which are Yobisin Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
Which are the Pharmacologic Classes for Yobisin?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
* Please review the disclaimer below.
[1] 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".