NDC 63083-5020 Pancreas Drops 5020
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-5020 - Pancreas Drops
Product Packages
NDC Code 63083-5020-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-5020?
What are the uses for Pancreas Drops 5020?
Which are Pancreas Drops 5020 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW)
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW) (Active Moiety)
- FOENICULUM VULGARE FRUIT (UNII: J5W36Y5WG8)
- FOENICULUM VULGARE FRUIT (UNII: J5W36Y5WG8) (Active Moiety)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK) (Active Moiety)
- SYZYGIUM CUMINI SEED (UNII: 820LSF646I)
- SYZYGIUM CUMINI SEED (UNII: 820LSF646I) (Active Moiety)
- BILBERRY (UNII: 9P2U39H18W)
- BILBERRY (UNII: 9P2U39H18W) (Active Moiety)
- ACETIC ACID (UNII: Q40Q9N063P)
- ACETIC ACID (UNII: Q40Q9N063P) (Active Moiety)
- MARSDENIA CUNDURANGO WHOLE (UNII: AT33ZFZ5A1)
- MARSDENIA CUNDURANGO WHOLE (UNII: AT33ZFZ5A1) (Active Moiety)
- KIDNEY BEAN (UNII: M98C8416QO)
- KIDNEY BEAN (UNII: M98C8416QO) (Active Moiety)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG) (Active Moiety)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
- BOS TAURUS PANCREAS (UNII: 1M529TNT1D)
- BOS TAURUS PANCREAS (UNII: 1M529TNT1D) (Active Moiety)
- PANCRELIPASE AMYLASE (UNII: YOJ58O116E)
- PANCRELIPASE AMYLASE (UNII: YOJ58O116E) (Active Moiety)
- UREA (UNII: 8W8T17847W)
- UREA (UNII: 8W8T17847W) (Active Moiety)
- URIC ACID (UNII: 268B43MJ25)
- URIC ACID (UNII: 268B43MJ25) (Active Moiety)
Which are Pancreas Drops 5020 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".