warnings
WARNINGS • For external use only
ECLIPSE SPF 50 ALL SHADES
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
- ECLIPSE SPF 50 ALL SHADES
- Generic name
- TITANIUM DIOXIDE, ZINC OXIDE
- Manufacturer
- SCIENCE OF SKINCARE LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 49df51e6-be9a-41be-b3e1-bfc062aaceaa
- SPL ID
- 2b4f813d-ef21-2f8e-e063-6394a90ab619
- Version
- 8
- Effective date
- 2025-01-09
- Source export date
- 2026-09-28
- 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/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:12:42
| 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 | ECLIPSE SPF 50 ALL SHADES | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | SCIENCE OF SKINCARE LLC | openfda.manufacturer_name | |
| ndc | package | 69219-102-21 | openfda.package_ndc |
| ndc | package | 69219-102-53 | openfda.package_ndc |
| ndc | package | 69219-102-51 | openfda.package_ndc |
| ndc | package | 69219-102-11 | openfda.package_ndc |
| ndc | package | 69219-102-03 | openfda.package_ndc |
| ndc | package | 69219-102-13 | openfda.package_ndc |
| ndc | package | 69219-102-01 | openfda.package_ndc |
| ndc | package | 69219-102-02 | openfda.package_ndc |
| ndc | product | 69219-102 | openfda.product_ndc |
| ndc11 | package | 69219010203 | derived:openfda.package_ndc |
| ndc11 | package | 69219010202 | derived:openfda.package_ndc |
| ndc11 | package | 69219010251 | derived:openfda.package_ndc |
| ndc11 | package | 69219010201 | derived:openfda.package_ndc |
| ndc11 | package | 69219010211 | derived:openfda.package_ndc |
| ndc11 | package | 69219010221 | derived:openfda.package_ndc |
| ndc11 | package | 69219010213 | derived:openfda.package_ndc |
| ndc11 | package | 69219010253 | derived:openfda.package_ndc |
| spl id | 2b4f813d-ef21-2f8e-e063-6394a90ab619 | id | |
| spl set id | 49df51e6-be9a-41be-b3e1-bfc062aaceaa | set_id | |
| unii | SOI2LOH54Z | openfda.unii | |
| 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.