END-ZIT - 68605-2001-2 - (SULFUR)

Alphabetical Index


Drug Information of END-ZIT

Product NDC: 68605-2001
Proprietary Name: END-ZIT
Non Proprietary Name: SULFUR
Active Ingredient(s): .05    g/mL & nbsp;   SULFUR
Administration Route(s): TOPICAL
Dosage Form(s): LOTION, AUGMENTED
Coding System: National Drug Codes(NDC)

Labeler Information of END-ZIT

Product NDC: 68605-2001
Labeler Name: ABBE Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040420

Package Information of END-ZIT

Package NDC: 68605-2001-2
Package Description: 14.78 mL in 1 BOTTLE, GLASS (68605-2001-2)

NDC Information of END-ZIT

NDC Code 68605-2001-2
Proprietary Name END-ZIT
Package Description 14.78 mL in 1 BOTTLE, GLASS (68605-2001-2)
Product NDC 68605-2001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SULFUR
Dosage Form Name LOTION, AUGMENTED
Route Name TOPICAL
Start Marketing Date 20040420
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name ABBE Laboratories, Inc.
Substance Name SULFUR
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of END-ZIT


General Information