Triple Antibiotic
- Product NDC
- 55315-192
- 11-digit product format
- 553150192
- Labeler code
- 55315
- Product ID
- 55315-192_39fcb533-84b6-361f-e063-6294a90a94b6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- bacitracin zinc, neomycin sulfate, polymyxin B sulfate, and pramoxine hydrochloride
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- FRED'S, INC.
- Application
- M004
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-03-31
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Triple Antibiotic
- Brand name suffix
- Plus Pain Relief
- Listing expiration
- 2026-12-31
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 |
|---|
| 55315-192-34 | Triple AntibioticPlus Pain Relief | 1 in 1 CARTON | OINTMENT | 1 | | 3 |
| 55315-192-34 | Triple AntibioticPlus Pain Relief | 14.2 g in 1 TUBE | OINTMENT | 14.2 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55315-192 | TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [FRED'S, INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20241107_a44db5d1-7a74-44aa-9aa7-6247e771aaf2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55315-192-34 | 55315019234 | 1 TUBE in 1 CARTON (55315-192-34) / 14.2 g in 1 TUBE | 1 tube | 2019-01-14 | 0000-00-00 | No | No | Current |