warnings
For external use only Do not use on damaged or broken sin When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
| Harmonized routes |
|---|
| TOPICAL |
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 | Lather Daily Defense Mineral SPF 45 Facial Sunscreen | openfda.brand_name | |
| generic name | ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Lather, Inc. | openfda.manufacturer_name | |
| ndc | package | 77394-204-02 | openfda.package_ndc |
| ndc | product | 77394-204 | openfda.product_ndc |
| ndc11 | package | 77394020402 | derived:openfda.package_ndc |
| spl id | 51a021e1-3c37-74e9-e063-6394a90a1523 | id | |
| spl set id | 50c732a0-b282-d61b-e063-6294a90aa76b | set_id | |
| unii | SOI2LOH54Z | openfda.unii |
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse event summaries are temporarily unavailable. Other product information remains available.