WL-AAE-Z-O-1032
- Product NDC
- 63931-4469
- Requested package NDC
- 63931-4469-1
- 11-digit product format
- 639314469
- Labeler code
- 63931
- Product ID
- 63931-4469_da5b2a1d-d711-4456-e053-2995a90a704e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Nanophase Technologies Corporation
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-03-16
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 132 mg/mL
- 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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63931-4469-1 | 63931446901 | 150000 mL in 1 DRUM (63931-4469-1) | 150000 ml | 2022-03-16 | 0000-00-00 | No | No | Current |