LANI AND KAI MINERAL SUNSCREEN
- Product NDC
- 71447-052
- 11-digit product format
- 714470052
- Labeler code
- 71447
- Product ID
- 71447-052_d38259d3-248c-6ae5-e053-2a95a90a8f0e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE, ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- LABORATOIRES DRUIDE INC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-01
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 2 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | 71447-052 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | 0efc9e666f02… | f202fb6c5f17… | ||
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 71447-052 | 71447-052-01 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | 0efc9e666f02… | f202fb6c5f17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 71447-052-01 | 71447005201 | 1 BOTTLE, PLASTIC in 1 BOX (71447-052-01) > 50 g in 1 BOTTLE, PLASTIC (71447-052-00) | 2021-03-01 | 0000-00-00 | No | No | Current |