NDC 63083-2102 Liver Formula 2102
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2102 - Liver Formula
Product Packages
NDC Code 63083-2102-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2102?
What are the uses for Liver Formula 2102?
Which are Liver Formula 2102 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN)
- SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN) (Active Moiety)
- CROCUS SATIVUS FLOWER (UNII: 00IF91KFKQ)
- CROCUS SATIVUS FLOWER (UNII: 00IF91KFKQ) (Active Moiety)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (Active Moiety)
- LEUZEA RHAPONTICA ROOT (UNII: 52360307SI)
- LEUZEA RHAPONTICA ROOT (UNII: 52360307SI) (Active Moiety)
- AKEBIA STEM (UNII: 531B9G152H)
- AKEBIA STEM (UNII: 531B9G152H) (Active Moiety)
- GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
- GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549) (Active Moiety)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P) (Active Moiety)
- FRITILLARIA DELAVAYI WHOLE (UNII: 3RDU1QQR8H)
- FRITILLARIA DELAVAYI WHOLE (UNII: 3RDU1QQR8H) (Active Moiety)
- ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30)
- ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30) (Active Moiety)
Which are Liver Formula 2102 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.
[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".