Dynarex Zinc Oxide
- Product NDC
- 67777-119
- Requested package NDC
- 67777-119-20
- 11-digit product format
- 677770119
- Labeler code
- 67777
- Product ID
- 67777-119_ee2777e6-235a-30bd-e053-2a95a90afae4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide Ointment
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Dynarex Corporation
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-03-27
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 250 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67777-119 | DYNAREX ZINC OXIDE (ZINC OXIDE OINTMENT) OINTMENT [DYNAREX CORPORATION] | 7 | Legacy NDC | 20241122_686729af-f96e-a860-e053-2a91aa0af575.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67777-119-20 | 67777011920 | 425 g in 1 JAR (67777-119-20) | 425 g | 2018-03-27 | 0000-00-00 | No | No | Current |