NDC 49281-561 - PENTACEL
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
- 49281-561
- Package NDCs from labels
- 49281-561-01
- Manufacturer
- Sanofi Vaccines US Inc. | Sanofi Vaccines Canada Ltd.
- Effective date
- 2026-04-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PENTACEL - Sanofi Vaccines US Inc. | Sanofi Vaccines Canada Ltd. | Sanofi Vaccines US Inc. | Sanofi Vaccines Canada Ltd. | 2026-04-28 | VACCINE LABEL |
| PENTACEL - A-S Medication Solutions | A-S Medication Solutions | 2025-05-16 | VACCINE LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49281-561-01 | PENTACEL | 0.5 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SUSPENSION | 2.5 mL | 26 [D'ag'U] in 0.5mL | 13 |
| 49281-561-01 | PENTACEL | 0.5 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SUSPENSION | 2.5 mL | 7 [D'ag'U] in 0.5mL | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49281-561 | PENTACEL (DIPHTHERIA AND TETANUS TOXOIDS AND ACELLULAR PERTUSSIS ADSORBED, INACTIVATED POLIOVIRUS AND HAEMOPHILUS B CONJUGATE (TETANUS TOXOID CONJUGATE) VACCINE) KIT [SANOFI PASTEUR INC.] | 9 | Unmatched | 20250403_67d5c665-ca88-49ba-b7d3-7145d9878cf0.zip |
| 49281-561 | PENTACEL (DIPHTHERIA AND TETANUS TOXOIDS AND ACELLULAR PERTUSSIS ADSORBED, INACTIVATED POLIOVIRUS AND HAEMOPHILUS B CONJUGATE (TETANUS TOXOID CONJUGATE) VACCINE) KIT [A-S MEDICATION SOLUTIONS] | 1 | Unmatched | 20250523_e7a819d7-a597-4c91-9078-7cd20ac34410.zip |
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 |
|---|---|---|---|---|---|---|
| Tripleantibioticapainscaritch | FAMILY WELLNESS BACITRACIN,NEOMYCIN,POLYMYXINB,PRAMOXINEHCL | Trifecta Pharmaceutical USA LLC | 935106c6-8a9e-07fa-e053-2a95a90a2484 | 2024-12-20 | Warnings | 19371312D4 |
| Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE , POLYMYXIN B SULFATE. | TRIFECTA PHARMACEUTICALS USA LLC | 00c52a31-9bfa-a8bf-e063-6294a90ac4d7 | 2024-12-20 | Warnings | 19371312D4 |
| Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE , POLYMYXIN B SULFATE | Trifecta Pharmaceuticals Usa Llc | d04b397c-1608-4fd9-be28-ef7285d6a996 | 2024-12-20 | Warnings | 19371312D4 |
| Tripleantibioticointmentandpainrelief | FAMILY WELLNESS BACITRACIN,NEOMYCIN,POLYMYXINB,PRAMOXINE | Trifecta Pharmaceutical USA LLC | 91575333-5268-5d8f-e053-2a95a90a7a89 | 2024-12-20 | Warnings | 19371312D4 |
| Premier Value Max Strength Antibiotic plus pain relief | PREMIER VALUE NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HCL | Pharmacy Value Alliance LLC | 9767821e-054b-3bd3-e053-2a95a90a4b0e | 2024-12-20 | Warnings | 19371312D4 |
| Premier Value Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE | Premier Value Alliance LLC. | ab843664-a1e0-6716-e053-2995a90a2063 | 2024-12-20 | Warnings | 19371312D4 |
| Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE | Premier Value Alliance LLC. | ab863d90-1a8f-3c1f-e053-2a95a90aa0a7 | 2024-12-20 | Warnings | 19371312D4 |
| Family Wellness First Aid Antibiotic | FAMILY WELLNESS BACITRACIN ZINC, POLYMYXIN B SULFATE | Trifecta Pharmaceuticals USA, LLC | 9157681a-3ed1-096e-e053-2a95a90a05e3 | 2024-12-18 | Warnings | 19371312D4 |
| Family Wellness Original | FAMILY WELLNESS BACITRACIN, NEOMYCIN, POLYMYXIN B | Trifecta Pharmaceuticals USA LLC. | 915759af-0d4f-6a87-e053-2a95a90acbd6 | 2024-12-18 | Warnings | 19371312D4 |
| Family Wellness Pain Scar Itch | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B, PRAMOXINE HCL | Trifecta Pharmaceutical USA LLC | 9e507ec5-310d-3a21-e053-2a95a90a15a6 | 2024-12-18 | Warnings | 19371312D4 |
| First Aid Antibiotic plus Burn Relief | BACITRACINZINC,NEOMYCINSULFATE,POLYMXINBSULFATE,PRAMOXINEHCI | Trifecta Pharmaceuticals USA LLC | 048871e2-c917-292d-e063-6394a90af130 | 2024-12-18 | Warnings | 19371312D4 |
| TheraCare Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE | Veridian Healthcare | 0c3fc798-9a97-5316-e063-6394a90a6830 | 2024-12-18 | Warnings | 19371312D4 |
| Fendall Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | afda6fc3-7615-b0be-e053-2995a90a6208 | 2024-12-10 | Warnings | 059QF0KO0R |
| OP First Aid Series TRIPLE ANTIBIOTIC | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE | Nantong Health & Beyond Hygienic Products Inc. | cadebf07-dd48-4855-8296-7a91e28d7123 | 2024-12-05 | Warnings | 19371312D4 |
| triple antibiotic and pain relief | BACITRACIN, NEOMYCIN, POLYMYXIN B, PRAMOXINE HYDROCHLORIDE | CVS Pharmacy | f0864d78-23e6-4e6c-bc67-7ba3e6dd862c | 2024-12-03 | Warnings | 19371312D4 |
| PhysiciansCare Ophthalmic Solution Eyewash Purified Water, 98.3% | PURIFIED WATER 98.3% | Acme United Corporation | 9248ee71-2d47-620d-e053-2995a90af5c8 | 2024-11-26 | Warnings | 059QF0KO0R |
| Neomycin and Polymyxin B Sulfates and Hydrocortisone | NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND HYDROCORTISONE | NuCare Pharmaceuticals,Inc. | 6296e2ed-336b-b9af-e053-2991aa0aae0c | 2024-11-26 | Warnings, Adverse reactions | 19371312D4 |
| PhysiciansCare Ophthalmic Solution Eyewash | PURIFIED WATER 98.3% | Acme United Corporation | cca454e0-b2bd-4215-bc06-426fcc3f7bd6 | 2024-11-26 | Warnings | 059QF0KO0R |
| PhysiciansCare Ophthalmic Solution Eyewash | PURIFIED WATER 98.3% | Acme United Corporation | d3812fa3-9334-464d-b50c-98548ff76727 | 2024-11-26 | Warnings | 059QF0KO0R |
| DANGTTEOL | MINERAL WATER | AQBC CO., LTD | 27db14a9-3812-433f-e063-6394a90a11e7 | 2024-11-26 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.