Mineral Based Foam Sunscreen Tinted
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
- Mineral Based Foam Sunscreen Tinted
- Generic name
- TITANIUM DIOXIDE, ZINC OXIDE
- Manufacturer
- KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 32465271-abb9-d03f-e063-6294a90a990e
- SPL ID
- 45757254-5c2b-e59e-e063-6394a90a54e5
- Version
- 2
- Effective date
- 2025-12-08
- Source export date
- 2026-10-27
- 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/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:49:51
| 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 | Mineral Based Foam Sunscreen Tinted | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | openfda.manufacturer_name | |
| ndc | package | 81679-210-04 | openfda.package_ndc |
| ndc | product | 81679-210 | openfda.product_ndc |
| ndc11 | package | 81679021004 | derived:openfda.package_ndc |
| spl id | 45757254-5c2b-e59e-e063-6394a90a54e5 | id | |
| spl set id | 32465271-abb9-d03f-e063-6294a90a990e | set_id | |
| unii | SOI2LOH54Z | openfda.unii | |
| unii | 15FIX9V2JP | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.