Product NDC: | 12745-146 |
Proprietary Name: | Scrubidine |
Non Proprietary Name: | POVIDONE IODINE |
Active Ingredient(s): | 8.64 g/100mL & nbsp; POVIDONE IODINE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 12745-146 |
Labeler Name: | Medical Chemical Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19770803 |
Package NDC: | 12745-146-02 |
Package Description: | 3785 mL in 1 BOTTLE, PLASTIC (12745-146-02) |
NDC Code | 12745-146-02 |
Proprietary Name | Scrubidine |
Package Description | 3785 mL in 1 BOTTLE, PLASTIC (12745-146-02) |
Product NDC | 12745-146 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | POVIDONE IODINE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 19770803 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medical Chemical Corporation |
Substance Name | POVIDONE-IODINE |
Strength Number | 8.64 |
Strength Unit | g/100mL |
Pharmaceutical Classes |