| Product NDC: | 67777-220 |
| Proprietary Name: | Bacitracin Zinc |
| Non Proprietary Name: | Bacitracin Zinc |
| Active Ingredient(s): | 500 [iU]/g & nbsp; Bacitracin Zinc |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67777-220 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091201 |
| Package NDC: | 67777-220-01 |
| Package Description: | 12 BOX in 1 CASE (67777-220-01) > 144 PACKET in 1 BOX > .9 g in 1 PACKET |
| NDC Code | 67777-220-01 |
| Proprietary Name | Bacitracin Zinc |
| Package Description | 12 BOX in 1 CASE (67777-220-01) > 144 PACKET in 1 BOX > .9 g in 1 PACKET |
| Product NDC | 67777-220 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacitracin Zinc |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20091201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | BACITRACIN ZINC |
| Strength Number | 500 |
| Strength Unit | [iU]/g |
| Pharmaceutical Classes |