warnings
Warnings For external use only
Medi-First Triple Antibiotic
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Medi-First Triple Antibiotic
- Generic name
- BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE
- Manufacturer
- Unifirst First Aid Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- bd432abc-fefb-1b4b-e053-2995a90acb18
- SPL ID
- 0f285855-9644-7e1d-e063-6394a90ae46f
- Version
- 6
- Effective date
- 2024-01-17
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:28:46
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M004 | openfda.application_number | |
| brand name | Medi-First Plus Triple Antibiotic | openfda.brand_name | |
| brand name | Medi-First Triple Antibiotic | openfda.brand_name | |
| generic name | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE | openfda.generic_name | |
| manufacturer name | Unifirst First Aid Corporation | openfda.manufacturer_name | |
| ndc | package | 47682-227-73 | openfda.package_ndc |
| ndc | package | 47682-227-12 | openfda.package_ndc |
| ndc | package | 47682-227-99 | openfda.package_ndc |
| ndc | package | 47682-938-73 | openfda.package_ndc |
| ndc | package | 47682-227-35 | openfda.package_ndc |
| ndc | product | 47682-227 | openfda.product_ndc |
| ndc | product | 47682-938 | openfda.product_ndc |
| ndc11 | package | 47682022773 | derived:openfda.package_ndc |
| ndc11 | package | 47682022799 | derived:openfda.package_ndc |
| ndc11 | package | 47682022735 | derived:openfda.package_ndc |
| ndc11 | package | 47682022712 | derived:openfda.package_ndc |
| ndc11 | package | 47682093873 | derived:openfda.package_ndc |
| rxcui | 204602 | openfda.rxcui | |
| spl id | 0f285855-9644-7e1d-e063-6394a90ae46f | id | |
| spl set id | bd432abc-fefb-1b4b-e053-2995a90acb18 | set_id | |
| unii | 89Y4M234ES | openfda.unii | |
| unii | 057Y626693 | openfda.unii | |
| unii | 19371312D4 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.