NDC 82797-129 Alfalfa Plus Ginseng Syrup
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 82797-129 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
Product Characteristics
Code Structure Chart
Product Details
What is NDC 82797-129?
What are the uses for Alfalfa Plus Ginseng Syrup?
Which are Alfalfa Plus Ginseng Syrup UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- CINCHONA OFFICINALIS WHOLE (UNII: 3SXM338GIQ)
- CINCHONA OFFICINALIS WHOLE (UNII: 3SXM338GIQ) (Active Moiety)
- PANAX GINSENG WHOLE (UNII: 9L5JEP7MES)
- PANAX GINSENG WHOLE (UNII: 9L5JEP7MES) (Active Moiety)
- FERRIC CITRATE ANHYDROUS (UNII: 63G354M39Z)
- FERRIC CATION (UNII: 91O4LML611) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- FERROUS SULFATE (UNII: 39R4TAN1VT)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- AVENA SATIVA WHOLE (UNII: 5P8D0Z74RG)
- AVENA SATIVA WHOLE (UNII: 5P8D0Z74RG) (Active Moiety)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T) (Active Moiety)
- ALFALFA (UNII: DJO934BRBD)
- ALFALFA (UNII: DJO934BRBD) (Active Moiety)
Which are Alfalfa Plus Ginseng Syrup 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:
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITOL SOLUTION 70% (UNII: 8KW3E207O2)
- SODIUM CYCLAMATE (UNII: 1I6F42RME1)
- GLYCERIN (UNII: PDC6A3C0OX)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
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[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".