NDC 61727-329 Cholestop
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61727 - Homeocare Laboratories
- 61727-329 - Cholestop
Product Packages
NDC Code 61727-329-21
Package Description: 4 g in 1 TUBE
Product Details
What is NDC 61727-329?
What are the uses for Cholestop?
Which are Cholestop UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARCTIUM LAPPA WHOLE (UNII: 73070DU1LA)
- ARCTIUM LAPPA WHOLE (UNII: 73070DU1LA) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CHOLESTEROL (UNII: 97C5T2UQ7J) (Active Moiety)
- CHRYSANTHELLUM INDICUM SUBSP. AFROAMERICANUM (UNII: 2GGZ8I3HGN)
- CHRYSANTHELLUM INDICUM SUBSP. AFROAMERICANUM (UNII: 2GGZ8I3HGN) (Active Moiety)
- SOLIDAGO CANADENSIS FLOWERING TOP (UNII: ZHL562L3PR)
- SOLIDAGO CANADENSIS FLOWERING TOP (UNII: ZHL562L3PR) (Active Moiety)
- TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C)
- TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C) (Active Moiety)
Which are Cholestop 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:
- SUCROSE (UNII: C151H8M554)
- LACTOSE (UNII: J2B2A4N98G)
* 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".