Product NDC: | 59779-085 |
Proprietary Name: | POVIDONE IODINE |
Non Proprietary Name: | POVIONE IODINE |
Active Ingredient(s): | 1 g/10g & nbsp; POVIONE IODINE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-085 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20080730 |
Package NDC: | 59779-085-99 |
Package Description: | 1 TUBE in 1 CARTON (59779-085-99) > 28.4 g in 1 TUBE |
NDC Code | 59779-085-99 |
Proprietary Name | POVIDONE IODINE |
Package Description | 1 TUBE in 1 CARTON (59779-085-99) > 28.4 g in 1 TUBE |
Product NDC | 59779-085 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | POVIONE IODINE |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20080730 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | POVIDONE-IODINE |
Strength Number | 1 |
Strength Unit | g/10g |
Pharmaceutical Classes |