NDC 63083-2031 Glucose Drops 2031
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2031?
What are the uses for Glucose Drops 2031?
Which are Glucose Drops 2031 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHROMIUM (UNII: 0R0008Q3JB)
- CHROMIUM (UNII: 0R0008Q3JB) (Active Moiety)
- OXOGLURIC ACID (UNII: 8ID597Z82X)
- OXOGLURIC ACID (UNII: 8ID597Z82X) (Active Moiety)
- CORN SYRUP (UNII: 9G5L16BK6N)
- CORN SYRUP (UNII: 9G5L16BK6N) (Active Moiety)
- FRUCTOSE (UNII: 6YSS42VSEV)
- FRUCTOSE (UNII: 6YSS42VSEV) (Active Moiety)
- MOMORDICA BALSAMINA WHOLE (UNII: P5JFB9U0GM)
- MOMORDICA BALSAMINA WHOLE (UNII: P5JFB9U0GM) (Active Moiety)
- BOS TAURUS PANCREAS (UNII: 1M529TNT1D)
- BOS TAURUS PANCREAS (UNII: 1M529TNT1D) (Active Moiety)
- PYRIDOXINE (UNII: KV2JZ1BI6Z)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- SUCROSE (UNII: C151H8M554)
- SUCROSE (UNII: C151H8M554) (Active Moiety)
- VANADIUM (UNII: 00J9J9XKDE)
- VANADIUM (UNII: 00J9J9XKDE) (Active Moiety)
- MANGANESE GLUCONATE (UNII: 9YY2F980SV)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB)
- MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F)
- GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (Active Moiety)
Which are Glucose Drops 2031 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* Please review the disclaimer below.
[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".