La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Sunscreen
La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Sunscreen is an FDA drug label for the active ingredient TITANIUM DIOXIDE AND ZINC OXIDE manufactured by L'Oreal USA Products Inc administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231213.
- Generic name
- TITANIUM DIOXIDE AND ZINC OXIDE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 49967-907
- Application
- M020
- Label effective
- 20231213
Active ingredients
Indications & Usage
Uses helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun
Dosage & Administration
Directions - shake well before use - apply generously 15 minutes before sun exposure - reapply: - after 40 minutes of swimming or sweating - immediately after towel drying - at least every 2 hours - Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: - limit time in the sun, especially from 10 a.m. - 2 p.m. - wear long-sleeved shirts, pants, hats and sunglasses - children under 6 months of age: Ask a doctor
Contraindications
Not available.
Warnings
Warnings For external use only
Adverse Reactions
Not available.