Product NDC: | 68016-013 |
Proprietary Name: | povidine iodine |
Non Proprietary Name: | povidine iodine |
Active Ingredient(s): | 10 mL/100mL & nbsp; povidine iodine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68016-013 |
Labeler Name: | Chain Drug Consortium, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110317 |
Package NDC: | 68016-013-94 |
Package Description: | 6 BOTTLE in 1 CASE (68016-013-94) > 236 mL in 1 BOTTLE |
NDC Code | 68016-013-94 |
Proprietary Name | povidine iodine |
Package Description | 6 BOTTLE in 1 CASE (68016-013-94) > 236 mL in 1 BOTTLE |
Product NDC | 68016-013 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | povidine iodine |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20110317 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Chain Drug Consortium, LLC |
Substance Name | POVIDONE-IODINE |
Strength Number | 10 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |