NDC 17856-1543 Potassium Chloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corp.
- 17856-1543 - Potassium Chloride
Product Characteristics
Product Packages
NDC Code 17856-1543-1
Package Description: 15 mL in 1 CUP, UNIT-DOSE
Product Details
What is NDC 17856-1543?
What are the uses for Potassium Chloride?
Which are Potassium Chloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
Which are Potassium Chloride 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Potassium Chloride?
- RxCUI: 312515 - potassium chloride 20 MEQ in 15 mL Oral Solution
- RxCUI: 312515 - potassium chloride 1.33 MEQ/ML Oral Solution
- RxCUI: 312515 - K+ Chloride 1.33 MEQ/ML Oral Solution
- RxCUI: 312515 - Pot Chloride 1.33 MEQ/ML Oral Solution
- RxCUI: 312515 - potassium chloride 1.5 GM per 15 ML Oral Solution
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[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".