NDC 21695-216 Antipyrine And Benzocaine
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What is NDC 21695-216?
What are the uses for Antipyrine And Benzocaine?
Which are Antipyrine And Benzocaine UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANTIPYRINE (UNII: T3CHA1B51H)
- ANTIPYRINE (UNII: T3CHA1B51H) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Antipyrine And Benzocaine 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- OXYQUINOLINE SULFATE (UNII: 61VUG75Y3P)
What is the NDC to RxNorm Crosswalk for Antipyrine And Benzocaine?
- RxCUI: 244309 - antipyrine 5.4 % / benzocaine 1.4 % Otic Solution
- RxCUI: 244309 - antipyrine 54 MG/ML / benzocaine 14 MG/ML Otic 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".