warnings
WARNINGS • For external use only
EXTREME PROTECT SPF 30
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
- EXTREME PROTECT SPF 30
- Generic name
- OCTINOXATE, ZINC OXIDE
- Manufacturer
- SCIENCE OF SKINCARE LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ecc4d304-e7e2-45b6-b9b2-2c64d3630860
- SPL ID
- 50c44fa3-d2c0-2939-e063-6394a90af3b5
- Version
- 11
- Effective date
- 2026-05-01
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:38:21
| 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 | EXTREME PROTECT SPF 30 | openfda.brand_name | |
| generic name | OCTINOXATE, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | SCIENCE OF SKINCARE LLC | openfda.manufacturer_name | |
| ndc | package | 69219-103-28 | openfda.package_ndc |
| ndc | package | 69219-103-55 | openfda.package_ndc |
| ndc | package | 69219-103-51 | openfda.package_ndc |
| ndc | package | 69219-103-13 | openfda.package_ndc |
| ndc | package | 69219-103-15 | openfda.package_ndc |
| ndc | package | 69219-103-02 | openfda.package_ndc |
| ndc | package | 69219-103-01 | openfda.package_ndc |
| ndc | product | 69219-103 | openfda.product_ndc |
| ndc11 | package | 69219010301 | derived:openfda.package_ndc |
| ndc11 | package | 69219010302 | derived:openfda.package_ndc |
| ndc11 | package | 69219010355 | derived:openfda.package_ndc |
| ndc11 | package | 69219010351 | derived:openfda.package_ndc |
| ndc11 | package | 69219010315 | derived:openfda.package_ndc |
| ndc11 | package | 69219010313 | derived:openfda.package_ndc |
| ndc11 | package | 69219010328 | derived:openfda.package_ndc |
| spl id | 50c44fa3-d2c0-2939-e063-6394a90af3b5 | id | |
| spl set id | ecc4d304-e7e2-45b6-b9b2-2c64d3630860 | set_id | |
| unii | SOI2LOH54Z | 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.