NDC 51672-2027-01 - Triple Antibiotic Plus Pain Relief
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
- 51672-2027
- Requested NDC
- 51672-2027-01
- Package NDCs from labels
- 51672-2027-1, 51672-2027-2, 51672-2027-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | GOPALDAS VISRAM AND COMPANY LIMITED
- Effective date
- 2026-06-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Triple Antibiotic Plus Pain Relief | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | GOPALDAS VISRAM AND COMPANY LIMITED | 2026-06-04 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2027-1 | Triple Antibiotic Plus Pain Relief | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-2027-1 | Triple Antibiotic Plus Pain Relief | 14.2 g in 1 TUBE | OINTMENT | 14.2 | 5 | |
| 51672-2027-2 | Triple Antibiotic Plus Pain Relief | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-2027-2 | Triple Antibiotic Plus Pain Relief | 28.4 g in 1 TUBE | OINTMENT | 28.4 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2027 | TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.] | 4 | Current NDC, Legacy NDC, 4 package rows | 20240201_4545c043-8e8e-4288-b4d8-e6ec9d72f979.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-2027-1 | GM - Gram | 51672-2027 | 893ea024-ab65-4e1d-9ab2-f03d576f84aa | 1 | 2012-07-24 |
| 51672-2027-2 | GM - Gram | 51672-2027 | fbed32bb-0345-4662-883d-68be60b2c8ff | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Neo-Synalar | NEOMYCIN SULFATE AND FLUOCINOLONE ACETONIDE | Eurofarma, Inc. | 1141956e-8a4c-4f80-95d1-f15bdb57fdf6 | 2026-03-18 | Warnings, Adverse reactions | 057Y626693 |
| Bacitracin Zinc and Polymyxin B Sulfate | BACITRACIN ZINC AND POLYMYXIN B SULFATE | A-S Medication Solutions | 51f6eac3-205e-4beb-8522-6ba2c593f350 | 2026-03-17 | Warnings, Adverse reactions | 89Y4M234ES 19371312D4 |
| Bacitracin | BACITRACIN | Preferred Pharmaceuticals Inc. | 2f115e22-10f5-47fe-85df-f59e4387a373 | 2026-03-16 | Warnings | M004 |
| Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE , POLYMYXIN B SULFATE. | ProStat First Aid, LLC. | 4cd49c65-e347-7589-e063-6394a90a53bd | 2026-03-12 | Warnings | M004 89Y4M234ES 057Y626693 19371312D4 |
| Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE , POLYMYXIN B SULFATE. | ProStat First Aid, LLC. | 4cc6d822-f383-2ceb-e063-6294a90aecc7 | 2026-03-11 | Warnings | M004 89Y4M234ES 057Y626693 19371312D4 |
| Ora Zen Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE | Orazen Inc | abbf8c34-87cb-4366-9840-7264a5114b54 | 2026-03-11 | Warnings | M004 89Y4M234ES 057Y626693 19371312D4 |
| FM-24 FOAMING | CHLOROXYLENOL | People's Janitorial Supply | b3c2e174-6099-ba08-e053-2995a90a7290 | 2026-03-10 | Warnings | M004 |
| Prequel Anti-Itch Solution Medicated Calming | MEDICATED CALMING LOTION | The Center Brands, LLC | 419fa45b-992b-676e-e063-6394a90add81 | 2026-03-09 | Warnings | 88AYB867L5 |
| doubleantibioticointment | BACITRACIN ZINC, POLYMYXIN B SULFATE | Trifecta Pharmaceuticals USA LLC | 4eb5202e-8e5b-6d31-e054-00144ff88e88 | 2026-03-04 | Warnings | M004 89Y4M234ES 19371312D4 |
| Calamine | CALAMINE, PRAMOXINE HCL | Amazon.com Services LLC | aceb0b10-8c90-4a06-8c47-cd1a2b4676a3 | 2026-03-03 | Warnings, Adverse reactions | 88AYB867L5 |
| Clear Anti-Itch | PRAMOXINE HCL, ZINC ACETATE | Old East Main Co. | 91df1434-bce6-4c6e-beee-cb5ec1cc8fff | 2026-03-02 | Warnings, Adverse reactions | 88AYB867L5 |
| Polymyxin B Sulfate and Trimethoprim | POLYMYXIN B SULFATE AND TRIMETHOPRIM SULFATE | Preferred Pharmaceuticals Inc. | 31a7ad1f-3f58-41a0-94f0-36674285bb61 | 2026-03-02 | Adverse reactions | 19371312D4 |
| Clear Anti-Itch | PRAMOXINE HCL, ZINC ACETATE | Chain Drug Marketing Association | 1ff6bd85-3658-47ea-b6ca-0eb5d8dbb693 | 2026-02-27 | Warnings, Adverse reactions | 88AYB867L5 |
| Calamine | CALAMINE, PRAMOXINE HCL | Chain Drug Marketing Association | 6c848b98-f01c-40f2-a9aa-2af76cb370c8 | 2026-02-27 | Warnings, Adverse reactions | 88AYB867L5 |
| Neomycin Sulfate | NEOMYCIN SULFATE | Chartwell RX, LLC | 0aa6947b-4739-4b00-be93-7303a5fc687d | 2026-02-27 | Boxed warning, Warnings, Adverse reactions | 057Y626693 |
| Neomycin and Polymyxin B Sulfates and Hydrocortisone | NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND HYDROCORTISONE | A-S Medication Solutions | 1185a82b-e731-456a-8fc1-d9f0fc1ab0bc | 2026-02-24 | Warnings, Adverse reactions | 057Y626693 19371312D4 |
| Clear Anti Itch | PRAMOXINE HCL, ZINC ACETATE | Better Living Brands, LLC | 1d491635-9605-44fa-9860-ea23e4e8b21c | 2026-02-23 | Warnings, Adverse reactions | 88AYB867L5 |
| Clear Anti-Itch | PRAMOXINE HCL, ZINC ACETATE | Perrigo Direct, Inc | cc0378f2-6d5f-47ec-b16a-64668b4c29cc | 2026-02-19 | Warnings, Adverse reactions | 88AYB867L5 |
| Calamine | CALAMINE, PRAMOXIND HCL | Perrigo Direct, Inc | 54a20ec9-ab86-4410-af94-e04393e9d4b3 | 2026-02-19 | Warnings, Adverse reactions | 88AYB867L5 |
| Clear Anti-Itch | PRAMOXINE HCL, ZINC ACETATE | Meijer, Inc. | fa8ae34c-7b68-454f-8a3b-0eaa93a34092 | 2026-02-19 | Warnings, Adverse reactions | 88AYB867L5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.