NDC 52731-7053 Liver Complex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52731 - Nova Homeopathic Therapeutics, Inc.
- 52731-7053 - Liver Complex
Product Packages
NDC Code 52731-7053-2
Package Description: 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE (52731-7053-1)
Product Details
What is NDC 52731-7053?
What are the uses for Liver Complex?
Which are Liver Complex UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILYBUM MARIANUM SEED (UNII: U946SH95EE)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- CYNARA SCOLYMUS LEAF (UNII: B71UA545DE)
- CYNARA SCOLYMUS LEAF (UNII: B71UA545DE) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C)
- TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C) (Active Moiety)
Which are Liver Complex 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)
* 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".