Benzo-jel
NDC 0404-0742
Product Information
Benzo-jel is a UNAPPROVED DRUG OTHER-approved product labeled by Henry Schein, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a red product. This product entry covers the primary NDC 0404-0742 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
Labeler & Regulatory Data
Marketing Timeline
Product Characteristics
Code Structure Chart
Product Details
What is NDC 0404-0742?
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are the Inactive Ingredients associated 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:
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for this product?
- RxCUI: 1053444 - BENZO-JEL 20 % Oral Gel
- RxCUI: 1053444 - benzocaine 0.2 MG/MG Oral Gel [Benzo-Jel]
- RxCUI: 1053444 - Benzo-Jel 0.2 MG/MG Oral Gel
- RxCUI: 1053444 - Benzo-Jel 20 % Oral Gel
- RxCUI: 238910 - benzocaine 20 % Oral Gel
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