Triple Antibiotic
- Product NDC
- 73659-010
- 11-digit product format
- 736590010
- Labeler code
- 73659
- Product ID
- 73659-010_ce564b3e-e7ab-716d-e053-2995a90aded4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Triple Antibiotic
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Rapid Care, Inc
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-12-15
- Marketing end
- 0000-00-00
- Substance
- POLYMYXIN B SULFATE; BACITRACIN ZINC; NEOMYCIN SULFATE
- Active strength
- 5000 [USP'U]/g; [USP'U]/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 73659-010-10 | Triple Antibiotic | 0.5 g in 1 PACKET | OINTMENT | 0.5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73659-010 | TRIPLE ANTIBIOTIC OINTMENT [RAPID CARE, INC] | 2 | Legacy NDC, 1 package rows | 20211016_b712c185-71db-62e7-e053-2a95a90a1dc7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73659-010-10 | 73659001010 | .5 g in 1 PACKET (73659-010-10) | 2020-12-15 | 0000-00-00 | No | No | Current |