La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Body Broad Spectrum SPF 50 Ultra Light Sunscreen
- Product NDC
- 69625-018
- 11-digit product format
- 696250018
- Labeler code
- 69625
- Product ID
- 69625-018_23fbe68c-41a6-45b1-aff4-86909b50d49e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Cosmetique Active Production
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-06-01
- Marketing end
- 2023-06-30
- Substance
- TITANIUM DIOXIDE
- Active strength
- 110 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69625-018-01 | 69625001801 | 1 TUBE in 1 CARTON (69625-018-01) > 125 mL in 1 TUBE | 1 tube | 2013-06-01 | 2023-06-30 | No | No | Current |