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Ultra Seal Bacitracin
Ultra Seal Bacitracin - 42213-400-28 - (BACITRACIN ZINC)
Drug Information of Ultra Seal Bacitracin
| Product NDC: | 42213-400 |
| Proprietary Name: | Ultra Seal Bacitracin |
| 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) |
Labeler Information of Ultra Seal Bacitracin
| Product NDC: | 42213-400 |
| Labeler Name: | Ultra Seal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111204 |
Package Information of Ultra Seal Bacitracin
| Package NDC: | 42213-400-28 |
| Package Description: | 1 TUBE in 1 CARTON (42213-400-28) > 28 g in 1 TUBE |
NDC Information of Ultra Seal Bacitracin
| NDC Code | 42213-400-28 |
| Proprietary Name | Ultra Seal Bacitracin |
| Package Description | 1 TUBE in 1 CARTON (42213-400-28) > 28 g in 1 TUBE |
| Product NDC | 42213-400 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BACITRACIN ZINC |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20111204 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultra Seal Corporation |
| Substance Name | BACITRACIN ZINC |
| Strength Number | 500 |
| Strength Unit | [iU]/g |
| Pharmaceutical Classes |
