warnings
Warnings For external use only. Do not use on damaged or broken skin. Stop use and ask a doctor if rash occurs. When using this product, keep out of eyes. Rinse with water to remove.
EVERY DAY MINERAL SUN SCREEN SPF 45
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
- EVERY DAY MINERAL SUN SCREEN SPF 45
- Generic name
- ZINC OXIDE
- Manufacturer
- Stream2Sea, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7ec4954f-7d60-405b-8bff-cb602fc44a4e
- SPL ID
- 34565934-f9ac-c46a-e063-6294a90ac885
- Version
- 7
- Effective date
- 2025-05-04
- Source export date
- 2026-11-06
- 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/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:42:40
| 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 | EVERY DAY MINERAL SUN SCREEN SPF 45 | openfda.brand_name | |
| generic name | ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Stream2Sea, LLC | openfda.manufacturer_name | |
| ndc | package | 69555-045-13 | openfda.package_ndc |
| ndc | package | 69555-045-11 | openfda.package_ndc |
| ndc | package | 69555-045-02 | openfda.package_ndc |
| ndc | package | 69555-045-18 | openfda.package_ndc |
| ndc | package | 69555-045-16 | openfda.package_ndc |
| ndc | package | 69555-045-19 | openfda.package_ndc |
| ndc | package | 69555-045-12 | openfda.package_ndc |
| ndc | package | 69555-045-10 | openfda.package_ndc |
| ndc | package | 69555-045-06 | openfda.package_ndc |
| ndc | package | 69555-045-20 | openfda.package_ndc |
| ndc | package | 69555-045-07 | openfda.package_ndc |
| ndc | package | 69555-045-17 | openfda.package_ndc |
| ndc | package | 69555-045-01 | openfda.package_ndc |
| ndc | package | 69555-045-03 | openfda.package_ndc |
| ndc | package | 69555-045-05 | openfda.package_ndc |
| ndc | package | 69555-045-15 | openfda.package_ndc |
| ndc | package | 69555-045-09 | openfda.package_ndc |
| ndc | package | 69555-045-04 | openfda.package_ndc |
| ndc | package | 69555-045-08 | openfda.package_ndc |
| ndc | package | 69555-045-14 | openfda.package_ndc |
| ndc | product | 69555-045 | openfda.product_ndc |
| ndc11 | package | 69555004507 | derived:openfda.package_ndc |
| ndc11 | package | 69555004508 | derived:openfda.package_ndc |
| ndc11 | package | 69555004516 | derived:openfda.package_ndc |
| ndc11 | package | 69555004501 | derived:openfda.package_ndc |
| ndc11 | package | 69555004518 | derived:openfda.package_ndc |
| ndc11 | package | 69555004513 | derived:openfda.package_ndc |
| ndc11 | package | 69555004505 | derived:openfda.package_ndc |
| ndc11 | package | 69555004503 | derived:openfda.package_ndc |
| ndc11 | package | 69555004520 | derived:openfda.package_ndc |
| ndc11 | package | 69555004512 | derived:openfda.package_ndc |
| ndc11 | package | 69555004506 | derived:openfda.package_ndc |
| ndc11 | package | 69555004514 | derived:openfda.package_ndc |
| ndc11 | package | 69555004511 | derived:openfda.package_ndc |
| ndc11 | package | 69555004519 | derived:openfda.package_ndc |
| ndc11 | package | 69555004510 | derived:openfda.package_ndc |
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.