WL-AAI-ZT-P-523
- Product NDC
- 63931-4318
- Requested package NDC
- 63931-4318-1
- 11-digit product format
- 639314318
- Labeler code
- 63931
- Product ID
- 63931-4318_f1ecfcdd-62ff-67ce-e053-2995a90a0eb8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium dioxide, Zinc Oxide
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Nanophase Technologies Corporation
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-07-15
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 0 g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|---|---|---|---|---|---|---|---|
| 63931-4318-1 | 63931431801 | 10000 g in 1 BAG (63931-4318-1) | 10000 g | 2019-07-15 | 0000-00-00 | No | No | Current |