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
- SICOS ET CIE
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 427a21cc-a668-4af8-94cb-b981d5c1919f
- SPL ID
- c52f341c-afa6-41ca-a7ad-ac2e6363c198
- Version
- 9
- Effective date
- 2024-06-25
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:09:53
| 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 | SICOS ET CIE | openfda.manufacturer_name | |
| ndc | package | 51150-142-01 | openfda.package_ndc |
| ndc | package | 51150-142-03 | openfda.package_ndc |
| ndc | package | 51150-142-04 | openfda.package_ndc |
| ndc | package | 51150-142-02 | openfda.package_ndc |
| ndc | product | 51150-142 | openfda.product_ndc |
| ndc11 | package | 51150014202 | derived:openfda.package_ndc |
| ndc11 | package | 51150014204 | derived:openfda.package_ndc |
| ndc11 | package | 51150014201 | derived:openfda.package_ndc |
| ndc11 | package | 51150014203 | derived:openfda.package_ndc |
| spl id | c52f341c-afa6-41ca-a7ad-ac2e6363c198 | id | |
| spl set id | 427a21cc-a668-4af8-94cb-b981d5c1919f | 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.