NDC 62565-903 One Touch Advanced Topical Anesthetic Bubble Gum

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
62565-903
Proprietary Name:
One Touch Advanced Topical Anesthetic Bubble Gum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hager Worldwide, Inc.
Labeler Code:
62565
Start Marketing Date: [9]
02-01-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - PURPLE)
Flavor(s):
BUBBLE GUM (C73368 - BUBBLE GUM)

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?

The NDC code 62565-903 is assigned by the FDA to the product One Touch Advanced Topical Anesthetic Bubble Gum which is product labeled by Hager Worldwide, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62565-903-01 1 jar in 1 box / 32 g in 1 jar. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for One Touch Advanced Topical Anesthetic Bubble Gum?

Indications OneTouch Advanced Gel is a topical anesthetic indicated for the productionof anesthesia of all accessible mucous membrane except the eyes. OneTouchAdvanced Gel is indicated for use to control pain in the mouth.

Which are One Touch Advanced Topical Anesthetic Bubble Gum UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for One Touch Advanced Topical Anesthetic Bubble Gum?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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.

Product Footnotes

[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".