warnings
Warnings For external use only
Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot 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
- Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment
- Generic name
- SULFUR
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 217c697e-0260-46d5-a202-ce7345eadd94
- SPL ID
- 1cb9aca2-b493-4ee2-85c9-0001329654fc
- Version
- 12
- Effective date
- 2023-12-30
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:09:28
| 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 | M006 | openfda.application_number | |
| brand name | Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment | openfda.brand_name | |
| generic name | SULFUR | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-895-04 | openfda.package_ndc |
| ndc | package | 49967-895-01 | openfda.package_ndc |
| ndc | package | 49967-895-03 | openfda.package_ndc |
| ndc | package | 49967-895-02 | openfda.package_ndc |
| ndc | product | 49967-895 | openfda.product_ndc |
| ndc11 | package | 49967089504 | derived:openfda.package_ndc |
| ndc11 | package | 49967089502 | derived:openfda.package_ndc |
| ndc11 | package | 49967089501 | derived:openfda.package_ndc |
| ndc11 | package | 49967089503 | derived:openfda.package_ndc |
| rxcui | 240725 | openfda.rxcui | |
| spl id | 1cb9aca2-b493-4ee2-85c9-0001329654fc | id | |
| spl set id | 217c697e-0260-46d5-a202-ce7345eadd94 | set_id | |
| unii | 70FD1KFU70 | 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.