NDC 61040-226 - First Aid Only Triple Antibiotic
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 61040-226
- Manufacturer
- Acme United Corporation
- Effective date
- 2024-11-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| First Aid Only Triple Antibiotic - Acme United Corporation | Acme United Corporation | 2024-11-19 | HUMAN OTC DRUG LABEL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Neomycin and Polymyxin B Sulfates and Hydrocortisone | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE | Proficient Rx LP | d55f1783-9c49-4f90-9ff8-6f132e7b325e | 2021-01-01 | Boxed warning, Warnings, Adverse reactions | 057Y626693 19371312D4 |
| Neomycin and Polymyxin B Sulfates and Dexamethasone | NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE | Proficient Rx LP | aa7b8a3f-06dd-4190-96a5-f86195bd2197 | 2021-01-01 | Warnings, Adverse reactions | 057Y626693 19371312D4 |
| Neomycin and Polymyxin B Sulfates and Hydrocortisone | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE | Asclemed USA, Inc. | 7c78ec84-8b7c-42f1-a879-3bf27a1daa71 | 2020-10-30 | Boxed warning, Warnings, Adverse reactions | 057Y626693 19371312D4 |
| Water-Jel 3-in-1 Antibiotic | BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE | Water-Jel Technologies | d5fcaffd-af38-4285-a79c-6df7424c76fa | 2017-11-16 | Warnings | 89Y4M234ES 057Y626693 19371312D4 |
| CVS Triple Antibiotic | BACITRACIN, NEOMYCIN, POLYMYXIN B | CVS Pharmacy | 454bfeed-f58f-003a-e054-00144ff8d46c | 2017-01-04 | Warnings | 204602 89Y4M234ES 057Y626693 19371312D4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.