Tinted Moisturizer SPF 30
- Product NDC
- 71692-001
- 11-digit product format
- 716920001
- Labeler code
- 71692
- Product ID
- 71692-001_f19b3f3c-4411-89ed-e053-2995a90a3981
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Titanium Dioxide, Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Regi U.S. Inc
- Application
- M020
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-09-08
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 8 g/100g; g/100g; g/100g
- 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.
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71692-001-35 | 71692000135 | 35 g in 1 TUBE (71692-001-35) | 35 g | 2017-09-08 | 0000-00-00 | No | No | Current |