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ULTRA SEAL Triple Antibiotic
ULTRA SEAL Triple Antibiotic - 42213-360-80 - (neomycin, polymixin, bacitracin)
Drug Information of ULTRA SEAL Triple Antibiotic
| Product NDC: | 42213-360 |
| Proprietary Name: | ULTRA SEAL Triple Antibiotic |
| Non Proprietary Name: | neomycin, polymixin, bacitracin |
| Active Ingredient(s): | 400; 5; 5000 [iU]/g; mg/g; [iU]/g & nbsp; neomycin, polymixin, bacitracin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ULTRA SEAL Triple Antibiotic
| Product NDC: | 42213-360 |
| Labeler Name: | Ultra Seal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110412 |
Package Information of ULTRA SEAL Triple Antibiotic
| Package NDC: | 42213-360-80 |
| Package Description: | 144 PACKET in 1 BOX (42213-360-80) > .9 g in 1 PACKET (42213-360-09) |
NDC Information of ULTRA SEAL Triple Antibiotic
| NDC Code | 42213-360-80 |
| Proprietary Name | ULTRA SEAL Triple Antibiotic |
| Package Description | 144 PACKET in 1 BOX (42213-360-80) > .9 g in 1 PACKET (42213-360-09) |
| Product NDC | 42213-360 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | neomycin, polymixin, bacitracin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110412 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultra Seal Corporation |
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 400; 5; 5000 |
| Strength Unit | [iU]/g; mg/g; [iU]/g |
| Pharmaceutical Classes |
