NDC 63083-2101 Esophagus Formula 2101
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2101 - Esophagus Formula
Product Packages
NDC Code 63083-2101-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2101?
What are the uses for Esophagus Formula 2101?
Which are Esophagus Formula 2101 UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLEDITSIA SINENSIS FRUIT (UNII: A6W0J6UO7Q)
- GLEDITSIA SINENSIS FRUIT (UNII: A6W0J6UO7Q) (Active Moiety)
- SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN)
- SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN) (Active Moiety)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
- ACHYRANTHES BIDENTATA ROOT (UNII: 5QIU26R6P1)
- ACHYRANTHES BIDENTATA ROOT (UNII: 5QIU26R6P1) (Active Moiety)
- RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M)
- RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M) (Active Moiety)
- AMMONIUM CATION (UNII: 54S68520I4)
- AMMONIUM CATION (UNII: 54S68520I4) (Active Moiety)
Which are Esophagus Formula 2101 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)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".