warnings
Warnings For external use only
Kiehls Since 1851 Ultra Facial Moisturizer Broad Spectrum SPF 30 Sunscreen For All Skin Types
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 Ultra Facial Moisturizer Broad Spectrum SPF 30 Sunscreen For All Skin Types
- Generic name
- AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d1a8c8d2-59d2-4389-9369-5f9b053a956e
- SPL ID
- e96dab17-d26d-4fb5-9e40-b88d0bdcbf7a
- Version
- 6
- Effective date
- 2023-12-30
- Source export date
- 2026-10-30
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:25:47
| 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 Ultra Facial Moisturizer Broad Spectrum SPF 30 Sunscreen For All Skin Types | 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 | 49967-797-01 | openfda.package_ndc |
| ndc | package | 49967-797-03 | openfda.package_ndc |
| ndc | package | 49967-797-02 | openfda.package_ndc |
| ndc | package | 49967-797-05 | openfda.package_ndc |
| ndc | package | 49967-797-04 | openfda.package_ndc |
| ndc | product | 49967-797 | openfda.product_ndc |
| ndc11 | package | 49967079703 | derived:openfda.package_ndc |
| ndc11 | package | 49967079704 | derived:openfda.package_ndc |
| ndc11 | package | 49967079701 | derived:openfda.package_ndc |
| ndc11 | package | 49967079705 | derived:openfda.package_ndc |
| ndc11 | package | 49967079702 | derived:openfda.package_ndc |
| spl id | e96dab17-d26d-4fb5-9e40-b88d0bdcbf7a | id | |
| spl set id | d1a8c8d2-59d2-4389-9369-5f9b053a956e | 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.