Home > National Drug Code (NDC) > BABY ANBESOL

BABY ANBESOL - 0573-0216-25 - (benzocaine)

Alphabetical Index


Drug Information of BABY ANBESOL

Product NDC: 0573-0216
Proprietary Name: BABY ANBESOL
Non Proprietary Name: benzocaine
Active Ingredient(s): 75    mg/g & nbsp;   benzocaine
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of BABY ANBESOL

Product NDC: 0573-0216
Labeler Name: Wyeth Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040401

Package Information of BABY ANBESOL

Package NDC: 0573-0216-25
Package Description: 1 TUBE in 1 BLISTER PACK (0573-0216-25) > 9 g in 1 TUBE

NDC Information of BABY ANBESOL

NDC Code 0573-0216-25
Proprietary Name BABY ANBESOL
Package Description 1 TUBE in 1 BLISTER PACK (0573-0216-25) > 9 g in 1 TUBE
Product NDC 0573-0216
Product Type Name HUMAN OTC DRUG
Non Proprietary Name benzocaine
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20040401
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Wyeth Consumer Healthcare
Substance Name BENZOCAINE
Strength Number 75
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of BABY ANBESOL


General Information