58232-4033 : Polysporin Topical Powder
| NDC: | 58232-4033 |
| Labeler: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | Human OTC Drug |
| Drug Name: |  Polysporin |
| Dosage Form: | Topical Powder |
| Application #: | part333 |
| Rev. Date: |
NDC Package Codes:
- 58232-4033-1: 1 BOTTLE IN 1 CARTON (58232‑4033‑1) > 10 G IN 1 BOTTLE
Active Ingredients:
- Polymyxin B Sulfate
- Bacitracin Zinc
Dosage Strength:
- 10000 [USP'U]/g
- 500 [USP'U]/g
Pharmaceutical Classes:
- Decreased Cell Wall Synthesis & Repair [PE]
- Polymyxin-class Antibacterial [EPC]
- Polymyxins [CS]
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.