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NDC 00904-8805-67 Major Triple Antibiotic 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g Details
Major Triple Antibiotic 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g
Major Triple Antibiotic is a TOPICAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by Major Pharmaceuticals. 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: 00904-8805-67Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Neomycin, Polymyxin, and Bacitracin Topical
Product Information
| NDC | 00904-8805 |
|---|---|
| Product ID | 0904-8805_0c9007ab-62cf-f258-e063-6394a90ac613 |
| Associated GPIs | 90109803104200 |
| GCN Sequence Number | 061415 |
| GCN Sequence Number Description | neomycin/bacitracin/polymyxinB OINT PACK 3.5-400-5K TOPICAL |
| HIC3 | Q5W |
| HIC3 Description | TOPICAL ANTIBIOTICS |
| GCN | 97206 |
| HICL Sequence Number | 033356 |
| HICL Sequence Number Description | NEOMYCIN SULFATE/BACITRACIN ZINC/POLYMYXIN B |
| Brand/Generic | Brand |
| Proprietary Name | Major Triple Antibiotic |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Bacitracin Zinc, Neomycin, Polymyxin B Sulfat |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | OINTMENT |
| Route | TOPICAL |
| Active Ingredient Strength | 400; 3.5; 5000 |
| Active Ingredient Units | [USP'U]/g; mg/g; [USP'U]/g |
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Labeler Name | Major Pharmaceuticals |
| 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 00904-8805-67 (00904880567)
| NDC Package Code | 0904-8805-67 |
|---|---|
| Billing NDC | 00904880567 |
| Package | 144 PACKET in 1 CARTON (0904-8805-67) / .9 g in 1 PACKET |
| Marketing Start Date | 2020-05-29 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |