Product NDC: | 17518-051 |
Proprietary Name: | 3M Avagard |
Non Proprietary Name: | Chlorhexidine Gluconate and Alcohol |
Active Ingredient(s): | 506.3; 8.3 mg/mL; mg/mL & nbsp; Chlorhexidine Gluconate and Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17518-051 |
Labeler Name: | 3M Health Care |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021074 |
Marketing Category: | NDA |
Start Marketing Date: | 20010614 |
Package NDC: | 17518-051-01 |
Package Description: | 8 BOTTLE in 1 CASE (17518-051-01) > 500 mL in 1 BOTTLE |
NDC Code | 17518-051-01 |
Proprietary Name | 3M Avagard |
Package Description | 8 BOTTLE in 1 CASE (17518-051-01) > 500 mL in 1 BOTTLE |
Product NDC | 17518-051 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Chlorhexidine Gluconate and Alcohol |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20010614 |
Marketing Category Name | NDA |
Labeler Name | 3M Health Care |
Substance Name | ALCOHOL; CHLORHEXIDINE GLUCONATE |
Strength Number | 506.3; 8.3 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |