warnings
Warnings For external use only
CeraVe Developed with Dermatologists Hydrating Sheer Sunscreen Broad Spectrum SPF 30 Face and Body Water Resistant 80 Minutes Hybrid Formula
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
- CeraVe Developed with Dermatologists Hydrating Sheer Sunscreen Broad Spectrum SPF 30 Face and Body Water Resistant 80 Minutes Hybrid Formula
- Generic name
- HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND ZINC OXIDE
- Manufacturer
- L'Oreal USA Products, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cd69df67-5231-4a75-a9fb-a8669806a892
- SPL ID
- 97f682ae-8958-4ce4-9fe7-30ca215087d5
- Version
- 3
- Effective date
- 2025-07-08
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:20:38
| 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 | CeraVe Developed with Dermatologists Hydrating Sheer Sunscreen Broad Spectrum SPF 30 Face and Body Water Resistant 80 Minutes Hybrid Formula | openfda.brand_name | |
| generic name | HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND ZINC OXIDE | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products, Inc. | openfda.manufacturer_name | |
| ndc | package | 49967-832-02 | openfda.package_ndc |
| ndc | package | 49967-832-01 | openfda.package_ndc |
| ndc | package | 49967-832-03 | openfda.package_ndc |
| ndc | product | 49967-832 | openfda.product_ndc |
| ndc11 | package | 49967083203 | derived:openfda.package_ndc |
| ndc11 | package | 49967083202 | derived:openfda.package_ndc |
| ndc11 | package | 49967083201 | derived:openfda.package_ndc |
| spl id | 97f682ae-8958-4ce4-9fe7-30ca215087d5 | id | |
| spl set id | cd69df67-5231-4a75-a9fb-a8669806a892 | set_id | |
| unii | 5A68WGF6WM | openfda.unii | |
| unii | V06SV4M95S | openfda.unii | |
| unii | SOI2LOH54Z | 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.