NDC 63083-2093 Stomach Enzyme Drops 2093
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2093 - Stomach Enzyme Drops
Product Packages
NDC Code 63083-2093-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2093?
What are the uses for Stomach Enzyme Drops 2093?
Which are Stomach Enzyme Drops 2093 UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANCRELIPASE AMYLASE (UNII: YOJ58O116E)
- PANCRELIPASE AMYLASE (UNII: YOJ58O116E) (Active Moiety)
- CELLULASE (TRICHODERMA LONGIBRACHIATUM) (UNII: 7Q170212NX)
- CELLULASE (TRICHODERMA LONGIBRACHIATUM) (UNII: 7Q170212NX) (Active Moiety)
- PANCRELIPASE LIPASE (UNII: 8MYC33932O)
- PANCRELIPASE LIPASE (UNII: 8MYC33932O) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- PEPSIN (UNII: GID333S43J)
- PEPSIN (UNII: GID333S43J) (Active Moiety)
- BETAINE HYDROCHLORIDE (UNII: JK8U8K4D6K)
- BETAINE (UNII: 3SCV180C9W) (Active Moiety)
- TRIPE (UNII: C46FS57S0X)
- TRIPE (UNII: C46FS57S0X) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
Which are Stomach Enzyme Drops 2093 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".