Triple Antibiotic
- Product NDC
- 67777-118
- 11-digit product format
- 677770118
- Labeler code
- 67777
- Product ID
- 67777-118_81558d4b-c9d1-5ccb-e053-2a91aa0a67f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- First Aid Antibiotic
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Dynarex Corporation
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-01-23
- Marketing end
- 0000-00-00
- Substance
- BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
- Active strength
- 400 1/1000mg; mg/1000mg; 1/1000mg
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 67777-118-40 | Triple Antibiotic | 72 in 1 CASE | OINTMENT | 72 | | 2 |
| 67777-118-40 | Triple Antibiotic | 14000 mg in 1 TUBE | OINTMENT | 14000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67777-118 | TRIPLE ANTIBIOTIC (FIRST AID ANTIBIOTIC) OINTMENT [DYNAREX CORPORATION] | 2 | Legacy NDC, 2 package rows | 20190208_7f941c9c-bccf-5b05-e053-2a91aa0a6e21.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 |
|---|
| 67777-118-40 | 67777011840 | 72 TUBE in 1 CASE (67777-118-40) > 14000 mg in 1 TUBE | 72 tube | 2018-01-23 | 0000-00-00 | No | No | Current |