warnings
Warnings For external use only
cle de peau BEAUTE THE FOUNDATION N M O20
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
- cle de peau BEAUTE THE FOUNDATION N M O20
- Generic name
- OCTINOXATE AND TITANIUM DIOXIDE
- Manufacturer
- Shiseido Americas Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 9507f6d1-c11c-428d-8d95-b436f27ba26a
- SPL ID
- 4b9306fc-0dca-4458-e063-6394a90acf85
- Version
- 2
- Effective date
- 2026-02-24
- Source export date
- 2026-10-12
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:29:41
| 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 |
|---|---|---|---|
| ndc | product | 58411-007 | openfda.product_ndc |
| ndc | product | 58411-011 | openfda.product_ndc |
| ndc | product | 58411-997 | openfda.product_ndc |
| ndc | product | 58411-012 | openfda.product_ndc |
| ndc | product | 58411-006 | openfda.product_ndc |
| ndc | product | 58411-009 | openfda.product_ndc |
| ndc | product | 58411-005 | openfda.product_ndc |
| ndc | product | 58411-002 | openfda.product_ndc |
| ndc11 | package | 58411000110 | derived:openfda.package_ndc |
| ndc11 | package | 58411001010 | derived:openfda.package_ndc |
| ndc11 | package | 58411099910 | derived:openfda.package_ndc |
| ndc11 | package | 58411000510 | derived:openfda.package_ndc |
| ndc11 | package | 58411000410 | derived:openfda.package_ndc |
| ndc11 | package | 58411000210 | derived:openfda.package_ndc |
| ndc11 | package | 58411099710 | derived:openfda.package_ndc |
| ndc11 | package | 58411000810 | derived:openfda.package_ndc |
| ndc11 | package | 58411000610 | derived:openfda.package_ndc |
| ndc11 | package | 58411001210 | derived:openfda.package_ndc |
| ndc11 | package | 58411000310 | derived:openfda.package_ndc |
| ndc11 | package | 58411001110 | derived:openfda.package_ndc |
| ndc11 | package | 58411000910 | derived:openfda.package_ndc |
| ndc11 | package | 58411000710 | derived:openfda.package_ndc |
| ndc11 | package | 58411099810 | derived:openfda.package_ndc |
| spl id | 4b9306fc-0dca-4458-e063-6394a90acf85 | id | |
| spl set id | 9507f6d1-c11c-428d-8d95-b436f27ba26a | set_id | |
| unii | 15FIX9V2JP | openfda.unii | |
| unii | 4Y5P7MUD51 | 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.