| 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: | 50353-102-10 |
| Package Description: | 1 BOTTLE, PUMP in 1 BLISTER PACK (50353-102-10) > 7.1 mL in 1 BOTTLE, PUMP |
| NDC Code | 50353-102-10 |
| Proprietary Name | Purmist |
| Package Description | 1 BOTTLE, PUMP in 1 BLISTER PACK (50353-102-10) > 7.1 mL in 1 BOTTLE, PUMP |
| 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 |