Product NDC: | 0519-1322 |
Proprietary Name: | Bactoshield CHG |
Non Proprietary Name: | Chlorhexidine Gluconate |
Active Ingredient(s): | 20 mg/mL & nbsp; Chlorhexidine Gluconate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0519-1322 |
Labeler Name: | STERIS Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA019422 |
Marketing Category: | NDA |
Start Marketing Date: | 19991004 |
Package NDC: | 0519-1322-08 |
Package Description: | 3708 mL in 1 BOTTLE (0519-1322-08) |
NDC Code | 0519-1322-08 |
Proprietary Name | Bactoshield CHG |
Package Description | 3708 mL in 1 BOTTLE (0519-1322-08) |
Product NDC | 0519-1322 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Chlorhexidine Gluconate |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19991004 |
Marketing Category Name | NDA |
Labeler Name | STERIS Corporation |
Substance Name | CHLORHEXIDINE GLUCONATE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes |