warnings
Warnings For external use only
La Roche Posay Laboratoire Dermatologique Anthelios Broad Spectrum SPF 100 Body and Face Melt In Milk Sunscreen Water Resistant 80 Minutes
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
- La Roche Posay Laboratoire Dermatologique Anthelios Broad Spectrum SPF 100 Body and Face Melt In Milk Sunscreen Water Resistant 80 Minutes
- Generic name
- AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 511f6de9-264a-4cf2-97c3-aa8adbc52a87
- SPL ID
- 54ee1697-fdfa-cf66-e063-6394a90a649f
- Version
- 4
- Effective date
- 2026-06-23
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:39:59
| 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 | La Roche Posay Laboratoire Dermatologique Anthelios Broad Spectrum SPF 100 Body and Face Melt In Milk Sunscreen Water Resistant 80 Minutes | 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 | 49967-103-02 | openfda.package_ndc |
| ndc | package | 49967-103-01 | openfda.package_ndc |
| ndc | package | 49967-103-03 | openfda.package_ndc |
| ndc | product | 49967-103 | openfda.product_ndc |
| ndc11 | package | 49967010301 | derived:openfda.package_ndc |
| ndc11 | package | 49967010303 | derived:openfda.package_ndc |
| ndc11 | package | 49967010302 | derived:openfda.package_ndc |
| spl id | 54ee1697-fdfa-cf66-e063-6394a90a649f | id | |
| spl set id | 511f6de9-264a-4cf2-97c3-aa8adbc52a87 | 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.