Product NDC: | 41250-110 |
Proprietary Name: | feminine |
Non Proprietary Name: | povidone-iodine |
Active Ingredient(s): | & nbsp; povidone-iodine |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41250-110 |
Labeler Name: | Meijer Distribution Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091104 |
Package NDC: | 41250-110-36 |
Package Description: | 1 KIT in 1 CARTON (41250-110-36) * 4 mL in 1 PACKET * 133 mL in 1 BOTTLE |
NDC Code | 41250-110-36 |
Proprietary Name | feminine |
Package Description | 1 KIT in 1 CARTON (41250-110-36) * 4 mL in 1 PACKET * 133 mL in 1 BOTTLE |
Product NDC | 41250-110 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | povidone-iodine |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20091104 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Meijer Distribution Inc |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |