Triple Antibiotic
- Product NDC
- 59640-801
- 11-digit product format
- 596400801
- Labeler code
- 59640
- Product ID
- 59640-801_b12de070-d7f8-415e-90b0-01c27feef8a4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bacitracin Zinc, Neomycin sulfate, Polymyxin B, Pramoxine Hydrochloride
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- H E B
- Application
- M004
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-02
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Triple Antibiotic
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BACITRACIN ZINC | 500 [USP'U]/g |
| NEOMYCIN SULFATE | 3.5 mg/g |
| POLYMYXIN B SULFATE | 10000 [USP'U]/g |
| PRAMOXINE HYDROCHLORIDE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 89Y4M234ES, 057Y626693, 19371312D4, 88AYB867L5 |
| Rxcui | 1359350 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59640-801-64 | Triple Antibiotic | 28 g in 1 TUBE | OINTMENT | 28 | | 3 |
| 59640-801-64 | Triple Antibiotic | 1 in 1 CARTON | OINTMENT | 1 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59640-801-64 | 59640080164 | 1 TUBE in 1 CARTON (59640-801-64) / 28 g in 1 TUBE | 1 tube | 2026-04-02 | No | No | Historical |