NDC 17856-0595 Sodium Citrate And Citric Acid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corp.
- 17856-0595 - Sodium Citrate And Citric Acid
Product Characteristics
Product Packages
NDC Code 17856-0595-4
Package Description: 1 CASE in 1 CUP, UNIT-DOSE / 50 CUP in 1 CASE (17856-0595-3) / 30 mL in 1 CUP
NDC Code 17856-0595-5
Package Description: 1 CASE in 1 CUP, UNIT-DOSE / 72 CUP, UNIT-DOSE in 1 CASE (17856-0595-1) / 15 mL in 1 CUP, UNIT-DOSE
Product Details
What is NDC 17856-0595?
What are the uses for Sodium Citrate And Citric Acid?
Which are Sodium Citrate And Citric Acid UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
Which are Sodium Citrate And Citric Acid 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:
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Sodium Citrate And Citric Acid?
- RxCUI: 543014 - citric acid 334 MG / sodium citrate 500 MG in 5 mL Oral Solution
- RxCUI: 543014 - citric acid 66.8 MG/ML / sodium citrate 100 MG/ML Oral Solution
- RxCUI: 543014 - citric acid 334 MG / sodium citrate 500 MG per 5 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".