Label: BENZO-JEL- benzocaine gel, dentifrice
-
Contains inactivated NDC Code(s)
NDC Code(s): 0404-3416-01 - Packager: Henry Schein, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 27, 2010
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- INGREDIENTS
- USUAL DOSAGE
- WARNING
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- CAUTION
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 29.6 mL Bottle Label
-
INGREDIENTS AND APPEARANCE
BENZO-JEL RASPBERRY
benzocaine gel, dentifriceProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0404-3416 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5) Benzocaine 220 mg in 1 g Product Characteristics Color Score Shape Size Flavor RASPBERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0404-3416-01 34 g in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 02/19/1963 Labeler - Henry Schein, Inc. (012430880) Registrant - DSHealthcare (056296981) Establishment Name Address ID/FEI Business Operations DENTSPLY Caulk 083235549 MANUFACTURE