warnings
Warnings For external use only
La Roche Posay Laboratoire Dermatologique Anthelios 60 Melt In Sunscreen Milk Broad Spectrum SPF 60 Face and Body
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 60 Melt In Sunscreen Milk Broad Spectrum SPF 60 Face and Body
- Generic name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE AND OXYBENZONE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 53ab6046-058b-4cdf-8e4e-7ce6f5288701
- SPL ID
- 0a19a27a-23ef-4072-8e73-d262d50ea95d
- Version
- 4
- Effective date
- 2023-12-31
- Source export date
- 2026-10-30
- 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/2026-10-30/eb45a4bb6908a5d117668eac8da5ce490c753c3f9b68298758ef131307d1d264/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:12:15
| 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 60 Melt In Sunscreen Milk Broad Spectrum SPF 60 Face and Body | openfda.brand_name | |
| generic name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE AND OXYBENZONE | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-003-01 | openfda.package_ndc |
| ndc | product | 49967-003 | openfda.product_ndc |
| ndc11 | package | 49967000301 | derived:openfda.package_ndc |
| spl id | 0a19a27a-23ef-4072-8e73-d262d50ea95d | id | |
| spl set id | 53ab6046-058b-4cdf-8e4e-7ce6f5288701 | set_id | |
| unii | 95OOS7VE0Y | openfda.unii | |
| 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.