| 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 |