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Bactoshield
Bactoshield - 0519-1364-09 - (CHLORHEXIDINE GLUCONATE)
Drug Information of Bactoshield
| Product NDC: | 0519-1364 |
| Proprietary Name: | Bactoshield |
| Non Proprietary Name: | CHLORHEXIDINE GLUCONATE |
| Active Ingredient(s): | 40 mg/mL & nbsp; CHLORHEXIDINE GLUCONATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPONGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bactoshield
| Product NDC: | 0519-1364 |
| Labeler Name: | STERIS Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019822 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030327 |
Package Information of Bactoshield
| Package NDC: | 0519-1364-09 |
| Package Description: | 1 APPLICATOR in 1 PACKAGE (0519-1364-09) > 25 mL in 1 APPLICATOR |
NDC Information of Bactoshield
| NDC Code | 0519-1364-09 |
| Proprietary Name | Bactoshield |
| Package Description | 1 APPLICATOR in 1 PACKAGE (0519-1364-09) > 25 mL in 1 APPLICATOR |
| Product NDC | 0519-1364 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CHLORHEXIDINE GLUCONATE |
| Dosage Form Name | SPONGE |
| Route Name | TOPICAL |
| Start Marketing Date | 20030327 |
| Marketing Category Name | NDA |
| Labeler Name | STERIS Corporation |
| Substance Name | CHLORHEXIDINE GLUCONATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
