Search by Drug Name or NDC
NDC 50814-0058-01 Genuine First Aid First Aid Antibiotic Bacitracin Zinc 400; 3.5; 5000 [iU]/g; mg/g; [iU]/g Details
Genuine First Aid First Aid Antibiotic Bacitracin Zinc 400; 3.5; 5000 [iU]/g; mg/g; [iU]/g
Genuine First Aid First Aid Antibiotic Bacitracin Zinc is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by GFA Production (Xiamen) Co., Ltd.. The primary component is BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE.
MedlinePlus Drug Summary
Neomycin, polymyxin, and bacitracin combination is used to prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Neomycin, polymyxin, and bacitracin are in a class of medications called antibiotics. Neomycin, polymyxin, and bacitracin combination works by stopping the growth of bacteria.
Related Packages: 50814-0058-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Neomycin, Polymyxin, and Bacitracin Topical
Product Information
| NDC | 50814-0058 |
|---|---|
| Product ID | 50814-058_0888da32-6074-7c47-e063-6394a90a01e8 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Genuine First Aid First Aid Antibiotic Bacitracin Zinc |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 400; 3.5; 5000 |
| Active Ingredient Units | [iU]/g; mg/g; [iU]/g |
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Labeler Name | GFA Production (Xiamen) Co., Ltd. |
| Pharmaceutical Class | Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Decreased Cell Wall Synthesis & Repair [PE], Polymyxin-class Antibacterial [EPC], Polymyxins [CS] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M004 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50814-0058-01 (50814005801)
| NDC Package Code | 50814-058-01 |
|---|---|
| Billing NDC | 50814005801 |
| Package | .9 g in 1 PACKAGE (50814-058-01) |
| Marketing Start Date | 2020-01-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |