NDC 51096-0001 Gluten Sensitivity Formula
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51096-0001?
What are the uses for Gluten Sensitivity Formula?
Which are Gluten Sensitivity Formula UNII Codes?
The UNII codes for the active ingredients in this product are:
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
Which are Gluten Sensitivity Formula 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:
- ARONIA MELANOCARPA FRUIT (UNII: S935718Z2Q)
- GELATIN (UNII: 2G86QN327L)
- ONCORHYNCHUS MASOU SPERM DNA (UNII: 1SI16O1B9R)
- FOLIC ACID (UNII: 935E97BOY8)
- CARNOSINE (UNII: 8HO6PVN24W)
- BROWN RICE (UNII: 659G217HPG)
- CYBERLINDNERA JADINII RNA (UNII: 5620EH64M4)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
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[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".