Triple Antibiotic
- Product NDC
- 67510-0170
- Requested package NDC
- 67510-0170-1
- 11-digit product format
- 675100170
- Labeler code
- 67510
- Product ID
- 67510-0170_b7b827d4-e5f8-6c44-e053-2995a90a4919
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bacitracin Zinc, Neomycin Sulfate, Polymyxin B
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Kareway Product, Inc.
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-08-10
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 67510-0170 | 67510-0170-1 | I | Inactivated by FDA | excluded / ndc_excluded.zip | e2bbac7714bc… | 27bdfed8d636… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 67510-0170-1 | 67510017001 | 1 TUBE in 1 BOX (67510-0170-1) > 28 g in 1 TUBE | 1 tube | 2011-08-11 | 0000-00-00 | No | No | Current |