NDC 51596-006 Critical Care Aspirin To Go
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51596 - Breakthrough Products Inc.
- 51596-006 - Critical Care Aspirin To Go
Product Characteristics
Product Packages
NDC Code 51596-006-01
Package Description: 1 POWDER in 1 POUCH
NDC Code 51596-006-05
Package Description: 5 POUCH in 1 BOX / 1 POWDER in 1 POUCH
NDC Code 51596-006-10
Package Description: 10 PACKET in 1 BOX / 1 POWDER in 1 PACKET
NDC Code 51596-006-12
Package Description: 12 POUCH in 1 BOX / 1 POWDER in 1 POUCH
NDC Code 51596-006-24
Package Description: 24 POUCH in 1 BOX / 1 POWDER in 1 POUCH
Product Details
What is NDC 51596-006?
What are the uses for Critical Care Aspirin To Go?
Which are Critical Care Aspirin To Go UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
Which are Critical Care Aspirin To Go 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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- DEXTROSE (UNII: IY9XDZ35W2)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Critical Care Aspirin To Go?
- RxCUI: 1050241 - aspirin 325 MG Oral Powder
- RxCUI: 1050241 - ASA 325 MG Oral Powder
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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".