Ulta
- Product NDC
- 58443-0393
- 11-digit product format
- 584430393
- Labeler code
- 58443
- Product ID
- 58443-0393_ca54fd0f-2e07-1447-e053-2a95a90ae7ce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Prime Enterprises, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-04
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 0 g/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 58443-0393-2 | 58443039302 | 20 g in 1 BOTTLE (58443-0393-2) | 20 g | 2021-03-04 | 0000-00-00 | No | No | Current |