NDC 27281-002 Livergen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 27281 - Sunway Biotech Llc
- 27281-002 - Livergen
Product Packages
NDC Code 27281-002-96
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 27281-002?
What are the uses for Livergen?
Which are Livergen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- SILYBUM MARIANUM SEED OIL (UNII: NYY23HEN06)
- SILYBUM MARIANUM SEED OIL (UNII: NYY23HEN06) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- HERRING SPERM DNA (UNII: 51FI676N6F)
- HERRING SPERM DNA (UNII: 51FI676N6F) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12)
- CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12) (Active Moiety)
- SUS SCROFA PANCREAS (UNII: 9Y3J3362RY)
- SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
Which are Livergen 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- 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.
[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".