Triple Antibiotic and Pain Relief
- Product NDC
- 11673-746
- 11-digit product format
- 116730746
- Labeler code
- 11673
- Product ID
- 11673-746_f358223c-786b-4113-9a59-f5b9dbb9b37d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Triple Antibiotic
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- M004
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-01-31
- Substance
- BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
- Active strength
- 500; 3.5; 10000; 10 [USP'U]/g; mg/g; [USP'U]/g; mg/g
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Decreased Cell Wall Synthesis & Repair [PE], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 89Y4M234ES | BACITRACIN ZINC | 1405-89-6 | BACITRACIN ZINC |
| 057Y626693 | NEOMYCIN SULFATE | 1405-10-3 | NEOMYCIN SULFATE |
| 19371312D4 | POLYMYXIN B SULFATE | 1405-20-5 | POLYMYXIN B SULFATE |
| 88AYB867L5 | PRAMOXINE HYDROCHLORIDE | 637-58-1 | PRAMOXINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 11673-746-28 | 11673074628 | 1 TUBE in 1 CARTON (11673-746-28) / 28 g in 1 TUBE | 1 tube | 2024-01-31 | No | No | Historical |