sunmark
- Product NDC
- 49348-600
- 11-digit product format
- 493480600
- Labeler code
- 49348
- Product ID
- 49348-600_39fd0345-f7e8-70ae-e063-6294a90a45c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- M004
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-03-31
- Marketing end
- 2027-08-31
- Substance
- BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
- Active strength
- 500; 3.5; 10000; 10 [iU]/g; mg/g; [iU]/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
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- sunmark
- Brand name suffix
- triple antibiotic plus pain relief
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BACITRACIN ZINC | 500 [iU]/g |
| NEOMYCIN SULFATE | 3.5 mg/g |
| POLYMYXIN B SULFATE | 10000 [iU]/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 |
|---|
| 49348-600-72 | sunmarktriple antibiotic plus pain relief | 1 in 1 CARTON | OINTMENT | 1 | | 4 |
| 49348-600-72 | sunmarktriple antibiotic plus pain relief | 28.4 g in 1 TUBE | OINTMENT | 28.4 | | 4 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| BACITRACIN ZINC | ACTIVE INGREDIENT | 89Y4M234ES | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
| NEOMYCIN SULFATE | ACTIVE INGREDIENT | 057Y626693 | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
| POLYMYXIN B SULFATE | ACTIVE INGREDIENT | 19371312D4 | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
| PRAMOXINE HYDROCHLORIDE | ACTIVE INGREDIENT | 88AYB867L5 | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
| BACITRACIN | ACTIVE MOIETY | 58H6RWO52I | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
| NEOMYCIN | ACTIVE MOIETY | I16QD7X297 | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
| POLYMYXIN B | ACTIVE MOIETY | J2VZ07J96K | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
| PRAMOXINE | ACTIVE MOIETY | 068X84E056 | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
| PETROLATUM | INACTIVE INGREDIENT | 4T6H12BN9U | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [MCKESSON] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49348-600 | SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [STRATEGIC SOURCING SERVICES LLC] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241006_941a6a71-e898-4af3-989a-6d3aa3224338.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 |
|---|
| 49348-600-72 | 49348060072 | 1 TUBE in 1 CARTON (49348-600-72) / 28.4 g in 1 TUBE | 1 tube | 2013-02-13 | 2027-08-31 | No | No | Current |