Benzo-Jel
BENZO-JEL™
Approved
Approval ID
07d8c4da-2c28-4aae-a129-03aae15b2991
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 27, 2010
Manufacturers
FDA
Henry Schein, Inc.
DUNS: 012430880
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Benzocaine
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0404-3416
Product Classification
G
Generic Name
Benzocaine
Product Specifications
Route of AdministrationDENTAL
Effective DateAugust 27, 2010
FDA Product Classification
INGREDIENTS (1)
BenzocaineActive
Quantity: 220 mg in 1 g
Code: U3RSY48JW5
Classification: ACTIB