warnings
Warnings For external use only
Kiehls Since 1851 Dermatologist Solutions SuperFluid UV Mineral Defense Broad Spectrum SPF 50 Plus Sunscreen
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 Dermatologist Solutions SuperFluid UV Mineral Defense Broad Spectrum SPF 50 Plus Sunscreen
- Generic name
- TITANIUM DIOXIDE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- eb43177e-389d-4572-8521-ee4d0a2dad3a
- SPL ID
- 9c24442b-9868-4269-b783-419171eda036
- Version
- 7
- Effective date
- 2023-12-30
- Source export date
- 2026-10-12
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:26:42
| 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 Dermatologist Solutions SuperFluid UV Mineral Defense Broad Spectrum SPF 50 Plus Sunscreen | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-409-04 | openfda.package_ndc |
| ndc | package | 49967-409-02 | openfda.package_ndc |
| ndc | package | 49967-409-01 | openfda.package_ndc |
| ndc | package | 49967-409-03 | openfda.package_ndc |
| ndc | product | 49967-409 | openfda.product_ndc |
| ndc11 | package | 49967040902 | derived:openfda.package_ndc |
| ndc11 | package | 49967040901 | derived:openfda.package_ndc |
| ndc11 | package | 49967040904 | derived:openfda.package_ndc |
| ndc11 | package | 49967040903 | derived:openfda.package_ndc |
| spl id | 9c24442b-9868-4269-b783-419171eda036 | id | |
| spl set id | eb43177e-389d-4572-8521-ee4d0a2dad3a | set_id | |
| unii | 15FIX9V2JP | 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.