warnings
Warnings For external use only
Lancome Paris Absolue Hand Premium Bx Broad Spectrum SPF 15 Sunscreen Absolute Anti Age Spot Unifying And Replenishing Treatment
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 Absolue Hand Premium Bx Broad Spectrum SPF 15 Sunscreen Absolute Anti Age Spot Unifying And Replenishing Treatment
- Generic name
- AVOBENZONE, OCTISALATE AND OCTOCRYLENE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 30cb2f12-1ebe-4850-be16-17748f0ba670
- SPL ID
- 2d5e9c53-a423-4502-a461-0fce452b5828
- Version
- 9
- Effective date
- 2023-12-30
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:34:50
| 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 Absolue Hand Premium Bx Broad Spectrum SPF 15 Sunscreen Absolute Anti Age Spot Unifying And Replenishing Treatment | openfda.brand_name | |
| generic name | AVOBENZONE, OCTISALATE AND OCTOCRYLENE | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-137-03 | openfda.package_ndc |
| ndc | package | 49967-137-02 | openfda.package_ndc |
| ndc | package | 49967-137-01 | openfda.package_ndc |
| ndc | package | 49967-137-04 | openfda.package_ndc |
| ndc | product | 49967-137 | openfda.product_ndc |
| ndc11 | package | 49967013702 | derived:openfda.package_ndc |
| ndc11 | package | 49967013704 | derived:openfda.package_ndc |
| ndc11 | package | 49967013703 | derived:openfda.package_ndc |
| ndc11 | package | 49967013701 | derived:openfda.package_ndc |
| spl id | 2d5e9c53-a423-4502-a461-0fce452b5828 | id | |
| spl set id | 30cb2f12-1ebe-4850-be16-17748f0ba670 | set_id | |
| unii | 5A68WGF6WM | 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.