LANCOME PARIS TEINT IDOLE ULTRA WEAR BROAD SPECTRUM SPF 25 BREATHABLE COVERAGE FOUNDATION SUNSCREEN
- Product NDC
- 51150-025
- 11-digit product format
- 511500025
- Labeler code
- 51150
- Product ID
- 51150-025_5c4f03ed-cc73-15f6-e063-6394a90a000a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate and Titanium Dioxide
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- SICOS ET CIE
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-25
- Substance
- OCTINOXATE; TITANIUM DIOXIDE
- Active strength
- 67; 36 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LANCOME PARIS TEINT IDOLE ULTRA WEAR BROAD SPECTRUM SPF 25 BREATHABLE COVERAGE FOUNDATION SUNSCREEN
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| OCTINOXATE | 67 mg/mL |
| TITANIUM DIOXIDE | 36 mg/mL |
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 | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 51150-025-01 | 51150002501 | 1 BOTTLE in 1 CARTON (51150-025-01) / 30 mL in 1 BOTTLE | 1 bottle | 2026-09-25 | No | No | Current |