NDC 60512-0010 Fatigue Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60512 - Homeolab Usa Inc.
- 60512-0010 - Fatigue Relief
Product Characteristics
Product Packages
NDC Code 60512-0010-1
Package Description: 80 PELLET in 1 TUBE
Product Details
What is NDC 60512-0010?
What are the uses for Fatigue Relief?
Which are Fatigue Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALFALFA WHOLE (UNII: DJO934BRBD)
- ALFALFA (UNII: DJO934BRBD) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- AVENA SATIVA LEAF (UNII: 206PI19V7R)
- AVENA SATIVA LEAF (UNII: 206PI19V7R) (Active Moiety)
- SELENIUM (UNII: H6241UJ22B)
- SELENIUM (UNII: H6241UJ22B) (Active Moiety)
- CHASTE TREE (UNII: 433OSF3U8A)
- CHASTE TREE (UNII: 433OSF3U8A) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
Which are Fatigue Relief 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".