NDC 63083-3003 B-balance Liquescence 3003
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-3003 - B-balance Liquescence
Product Packages
NDC Code 63083-3003-4
Package Description: 118 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-3003?
What are the uses for B-balance Liquescence 3003?
Which are B-balance Liquescence 3003 UNII Codes?
The UNII codes for the active ingredients in this product are:
- LATIGLUTENASE (UNII: 090PL12YZJ)
- LATIGLUTENASE (UNII: 090PL12YZJ) (Active Moiety)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) (Active Moiety)
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
- THIAMINE (UNII: X66NSO3N35)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- BEEF HEART (UNII: P47W069U38)
- BEEF HEART (UNII: P47W069U38) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- PYRIDOXINE (UNII: KV2JZ1BI6Z)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
Which are B-balance Liquescence 3003 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".