NDC 63083-2164 Secretin Cycle Ii Drops 2164
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2164 - Secretin Cycle Ii Drops
Product Packages
NDC Code 63083-2164-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2164?
What are the uses for Secretin Cycle Ii Drops 2164?
Which are Secretin Cycle Ii Drops 2164 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- BOS TAURUS BRAIN (UNII: A1YEE2DB8Z)
- BOS TAURUS BRAIN (UNII: A1YEE2DB8Z) (Active Moiety)
- BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7)
- BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (Active Moiety)
- BOS TAURUS LARGE INTESTINE (UNII: D176AZC57O)
- BOS TAURUS LARGE INTESTINE (UNII: D176AZC57O) (Active Moiety)
- BEEF KIDNEY (UNII: 5HOC10FSIC)
- BEEF KIDNEY (UNII: 5HOC10FSIC) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV) (Active Moiety)
- BOS TAURUS SPLEEN (UNII: 190Q9MB3U3)
- BOS TAURUS SPLEEN (UNII: 190Q9MB3U3) (Active Moiety)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE) (Active Moiety)
- SECRETIN, UNSPECIFIED (UNII: 88C55N56UU)
- SECRETIN, UNSPECIFIED (UNII: 88C55N56UU) (Active Moiety)
Which are Secretin Cycle Ii Drops 2164 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".