Product NDC: | 17271-506 |
Proprietary Name: | BD E-Z Scrub |
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: | 17271-506 |
Labeler Name: | Becton Dickinson and Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA019422 |
Marketing Category: | NDA |
Start Marketing Date: | 20010401 |
Package NDC: | 17271-506-02 |
Package Description: | 6 BOTTLE in 1 BOX (17271-506-02) > 946 mL in 1 BOTTLE |
NDC Code | 17271-506-02 |
Proprietary Name | BD E-Z Scrub |
Package Description | 6 BOTTLE in 1 BOX (17271-506-02) > 946 mL in 1 BOTTLE |
Product NDC | 17271-506 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | chlorhexidine gluconate |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20010401 |
Marketing Category Name | NDA |
Labeler Name | Becton Dickinson and Company |
Substance Name | CHLORHEXIDINE GLUCONATE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes |