Triple Antibiotic
- Product NDC
- 21695-194
- 11-digit product format
- 216950194
- Labeler code
- 21695
- Product ID
- 21695-194_75ab9c13-3227-4f20-a8a1-891a4380c085
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Neomycin and Polymyxin B Sulfates and Bacitracin Zinc
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Rebel Distributors Corp
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-01-06
- Marketing end
- 0000-00-00
- Substance
- BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
- Active strength
- 400 [USP'U]/g; mg/g; [USP'U]/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-194-15 | Triple Antibiotic | 15 g in 1 TUBE | OINTMENT | 15 | | 1 |
| 21695-194-15 | Triple Antibiotic | 1 in 1 CARTON | OINTMENT | 1 | | 1 |
| 21695-194-28 | Triple Antibiotic | 28 g in 1 TUBE | OINTMENT | 28 | | 1 |
| 21695-194-28 | Triple Antibiotic | 1 in 1 CARTON | OINTMENT | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-194 | TRIPLE ANTIBIOTIC (NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC) OINTMENT [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 4 package rows | 20110211_75ab9c13-3227-4f20-a8a1-891a4380c085.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 21695-194-15 | 21695019415 | 15 g in 1 TUBE | 15 g | Historical |
| 21695-194-28 | 21695019428 | 28 g in 1 TUBE | 28 g | Historical |