warnings
Warnings For external use only
Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 50 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
- Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 50 Sunscreen Water Resistant 80 MInutes
- Generic name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE AND OXYBENZONE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 04fd0839-5046-4633-a919-6b7b6bea4f3e
- SPL ID
- d746b613-5513-42fa-b219-c562f9fbc503
- Version
- 4
- Effective date
- 2023-12-30
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:36:51
| 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 | Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 50 Sunscreen Water Resistant 80 MInutes | 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 | 49967-047-01 | openfda.package_ndc |
| ndc | product | 49967-047 | openfda.product_ndc |
| ndc11 | package | 49967004701 | derived:openfda.package_ndc |
| spl id | d746b613-5513-42fa-b219-c562f9fbc503 | id | |
| spl set id | 04fd0839-5046-4633-a919-6b7b6bea4f3e | 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.