Product NDC: | 50353-102 |
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) |
Product NDC: | 50353-102 |
Labeler Name: | MKR International Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 50353-102-50 |
Package Description: | 6 BOTTLE, SPRAY in 1 CARTON (50353-102-50) > 100 mL in 1 BOTTLE, SPRAY |
NDC Code | 50353-102-50 |
Proprietary Name | Purmist |
Package Description | 6 BOTTLE, SPRAY in 1 CARTON (50353-102-50) > 100 mL in 1 BOTTLE, SPRAY |
Product NDC | 50353-102 |
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 |