NDC 63083-1015 Sugar Mix 1015
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-1015 - Sugar Mix
Product Packages
NDC Code 63083-1015-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-1015?
What are the uses for Sugar Mix 1015?
Which are Sugar Mix 1015 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)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- ASPARTAME (UNII: Z0H242BBR1)
- ASPARTAME (UNII: Z0H242BBR1) (Active Moiety)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) (Active Moiety)
- FRUCTOSE (UNII: 6YSS42VSEV)
- FRUCTOSE (UNII: 6YSS42VSEV) (Active Moiety)
- HONEY (UNII: Y9H1V576FH)
- HONEY (UNII: Y9H1V576FH) (Active Moiety)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) (Active Moiety)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MALTODEXTRIN (UNII: 7CVR7L4A2D) (Active Moiety)
- MALTOSE ANHYDROUS (UNII: 66Y63L379N)
- MALTOSE ANHYDROUS (UNII: 66Y63L379N) (Active Moiety)
- MOLASSES (UNII: LSU3YX0KZO)
- MOLASSES (UNII: LSU3YX0KZO) (Active Moiety)
- SACCHARIN (UNII: FST467XS7D)
- SACCHARIN (UNII: FST467XS7D) (Active Moiety)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SUCRALOSE (UNII: 96K6UQ3ZD4) (Active Moiety)
- SUCROSE (UNII: C151H8M554)
- SUCROSE (UNII: C151H8M554) (Active Moiety)
- LIGHT BROWN SUGAR (UNII: 8DUZ1N7T79)
- LIGHT BROWN SUGAR (UNII: 8DUZ1N7T79) (Active Moiety)
- SUCROSE STEARATE (UNII: 274KW0O50M)
- SUCROSE STEARATE (UNII: 274KW0O50M) (Active Moiety)
Which are Sugar Mix 1015 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".