Phisohex - 0024-1535-02 - (hexachlorophene)

Alphabetical Index


Drug Information of Phisohex

Product NDC: 0024-1535
Proprietary Name: Phisohex
Non Proprietary Name: hexachlorophene
Active Ingredient(s): 30    mg/mL & nbsp;   hexachlorophene
Administration Route(s): TOPICAL
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of Phisohex

Product NDC: 0024-1535
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA006882
Marketing Category: NDA
Start Marketing Date: 19760611

Package Information of Phisohex

Package NDC: 0024-1535-02
Package Description: 148 mL in 1 BOTTLE, PLASTIC (0024-1535-02)

NDC Information of Phisohex

NDC Code 0024-1535-02
Proprietary Name Phisohex
Package Description 148 mL in 1 BOTTLE, PLASTIC (0024-1535-02)
Product NDC 0024-1535
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hexachlorophene
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 19760611
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name HEXACHLOROPHENE
Strength Number 30
Strength Unit mg/mL
Pharmaceutical Classes Antiseptic [EPC]

Complete Information of Phisohex


General Information