Purmist - 50353-101-10 - (CHLORHEXIDINE GLUCONATE, ETHYL ALCOHOL)

Alphabetical Index


Drug Information of Purmist

Product NDC: 50353-101
Proprietary Name: Purmist
Non Proprietary Name: CHLORHEXIDINE GLUCONATE, ETHYL ALCOHOL
Active Ingredient(s): .7; .01    g/mL; g/mL & nbsp;   CHLORHEXIDINE GLUCONATE, ETHYL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Purmist

Product NDC: 50353-101
Labeler Name: MKR International Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100601

Package Information of Purmist

Package NDC: 50353-101-10
Package Description: 1 BOTTLE, PUMP in 1 BLISTER PACK (50353-101-10) > 7.1 mL in 1 BOTTLE, PUMP

NDC Information of Purmist

NDC Code 50353-101-10
Proprietary Name Purmist
Package Description 1 BOTTLE, PUMP in 1 BLISTER PACK (50353-101-10) > 7.1 mL in 1 BOTTLE, PUMP
Product NDC 50353-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CHLORHEXIDINE GLUCONATE, ETHYL ALCOHOL
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20100601
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name MKR International Inc
Substance Name ALCOHOL; CHLORHEXIDINE GLUCONATE
Strength Number .7; .01
Strength Unit g/mL; g/mL
Pharmaceutical Classes

Complete Information of Purmist


General Information