NDC 61509-105 Mark 3
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 61509-105?
What are the uses for Mark 3?
Which are Mark 3 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Mark 3 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:
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- XYLITOL (UNII: VCQ006KQ1E)
What is the NDC to RxNorm Crosswalk for Mark 3?
- RxCUI: 238910 - benzocaine 20 % Oral Gel
- RxCUI: 238910 - benzocaine 0.2 MG/MG Oral Gel
- RxCUI: 238910 - benzocaine 20 % (180-220 MG per 1 GM) Oral Gel
* Please review the disclaimer below.
[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".