warnings
Warnings For external use only
Lancome Paris UV Expert Aquagel Defense 50 Plus Sunscreen Broad Spectrum SPF 50 Plus Primer and Moisturizer
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Lancome Paris UV Expert Aquagel Defense 50 Plus Sunscreen Broad Spectrum SPF 50 Plus Primer and Moisturizer
- Generic name
- AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c88e44da-0b0e-4744-8b4b-4d9d418f29d7
- SPL ID
- 8b9615c9-7f34-4e0f-9e38-53ab4c4db7f0
- Version
- 8
- Effective date
- 2025-03-18
- Source export date
- 2026-11-06
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/423686b2ac39507df6931677ae004637f2f017f82cbe44b047a75ba358b9d453/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:58:06
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M020 | openfda.application_number | |
| brand name | Lancome Paris UV Expert Aquagel Defense 50 Plus Sunscreen Broad Spectrum SPF 50 Plus Primer and Moisturizer | openfda.brand_name | |
| generic name | AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-142-04 | openfda.package_ndc |
| ndc | package | 49967-142-01 | openfda.package_ndc |
| ndc | package | 49967-142-03 | openfda.package_ndc |
| ndc | package | 49967-142-05 | openfda.package_ndc |
| ndc | package | 49967-142-02 | openfda.package_ndc |
| ndc | product | 49967-142 | openfda.product_ndc |
| ndc11 | package | 49967014205 | derived:openfda.package_ndc |
| ndc11 | package | 49967014201 | derived:openfda.package_ndc |
| ndc11 | package | 49967014204 | derived:openfda.package_ndc |
| ndc11 | package | 49967014203 | derived:openfda.package_ndc |
| ndc11 | package | 49967014202 | derived:openfda.package_ndc |
| spl id | 8b9615c9-7f34-4e0f-9e38-53ab4c4db7f0 | id | |
| spl set id | c88e44da-0b0e-4744-8b4b-4d9d418f29d7 | set_id | |
| unii | 5A68WGF6WM | openfda.unii | |
| unii | V06SV4M95S | openfda.unii | |
| unii | G63QQF2NOX | openfda.unii | |
| unii | 4X49Y0596W | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.