NDC 62565-903 One Touch Advanced Topical Anesthetic Bubble Gum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62565 - Hager Worldwide, Inc.
- 62565-903 - One Touch Advanced Topical Anesthetic
Product Characteristics
Product Packages
NDC Code 62565-903-01
Package Description: 1 JAR in 1 BOX / 32 g in 1 JAR
Product Details
What is NDC 62565-903?
What are the uses for One Touch Advanced Topical Anesthetic Bubble Gum?
Which are One Touch Advanced Topical Anesthetic Bubble Gum UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- BUTAMBEN (UNII: EFW857872Q)
- BUTAMBEN (UNII: EFW857872Q) (Active Moiety)
- TETRACAINE HYDROCHLORIDE (UNII: 5NF5D4OPCI)
- TETRACAINE (UNII: 0619F35CGV) (Active Moiety)
Which are One Touch Advanced Topical Anesthetic Bubble Gum 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
What is the NDC to RxNorm Crosswalk for One Touch Advanced Topical Anesthetic Bubble Gum?
- RxCUI: 308645 - benzocaine 14 % / butamben 2 % / tetracaine 2 % Topical Gel
- RxCUI: 308645 - benzocaine 0.14 MG/MG / butamben 0.02 MG/MG / tetracaine 0.02 MG/MG Topical Gel
- RxCUI: 885585 - OneTouch Advanced 14 % / 2 % / 2 % Topical Gel
- RxCUI: 885585 - benzocaine 0.14 MG/MG / butamben 0.02 MG/MG / tetracaine 0.02 MG/MG Topical Gel [One Touch Reformulated Apr 2009]
- RxCUI: 885585 - One Touch Reformulated Apr 2009 14 % / 2 % / 2 % Mucous Membrane Topical 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".