NDC 63083-2094 Ulcer Drops 2094
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2094?
What are the uses for Ulcer Drops 2094?
Which are Ulcer Drops 2094 UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- STARCH, RICE (UNII: 4DGK8B7I3S)
- STARCH, RICE (UNII: 4DGK8B7I3S) (Active Moiety)
- PANICUM MILIACEUM WHOLE (UNII: 072D7X60WS)
- PANICUM MILIACEUM WHOLE (UNII: 072D7X60WS) (Active Moiety)
- PLANTAGO LANCEOLATA LEAF (UNII: 2YWL9J7EE8)
- PLANTAGO LANCEOLATA LEAF (UNII: 2YWL9J7EE8) (Active Moiety)
- FU LING (UNII: XH37TWY5O4)
- FU LING (UNII: XH37TWY5O4) (Active Moiety)
- DAIKON (UNII: 86R5J6D01D)
- DAIKON (UNII: 86R5J6D01D) (Active Moiety)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D) (Active Moiety)
- ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W)
- ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- HELICOBACTER PYLORI (UNII: U09W5JOL3Z)
- HELICOBACTER PYLORI (UNII: U09W5JOL3Z) (Active Moiety)
Which are Ulcer Drops 2094 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.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".