Bacti-Foam - 47593-169-41 - (Triclosan)

Alphabetical Index


Drug Information of Bacti-Foam

Product NDC: 47593-169
Proprietary Name: Bacti-Foam
Non Proprietary Name: Triclosan
Active Ingredient(s): 3    mg/mL & nbsp;   Triclosan
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bacti-Foam

Product NDC: 47593-169
Labeler Name: Ecolab Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19970711

Package Information of Bacti-Foam

Package NDC: 47593-169-41
Package Description: 750 mL in 1 BOTTLE, PLASTIC (47593-169-41)

NDC Information of Bacti-Foam

NDC Code 47593-169-41
Proprietary Name Bacti-Foam
Package Description 750 mL in 1 BOTTLE, PLASTIC (47593-169-41)
Product NDC 47593-169
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Triclosan
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 19970711
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ecolab Inc.
Substance Name TRICLOSAN
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Bacti-Foam


General Information