NDC 62565-802 Onetouch Revolution Topical Anesthetic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62565 - Hager Worldwide, Inc.
- 62565-802 - Onetouch Revolution
Product Characteristics
Product Packages
NDC Code 62565-802-01
Package Description: 32 g in 1 JAR
Product Details
What is NDC 62565-802?
What are the uses for Onetouch Revolution Topical Anesthetic?
Which are Onetouch Revolution Topical Anesthetic UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Onetouch Revolution Topical Anesthetic 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Onetouch Revolution Topical Anesthetic?
- 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".