Non Tinted Mineral Sunscreen
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
- Non Tinted Mineral Sunscreen
- Generic name
- TITANIUM DIOXIDE, ZINC OXIDE
- Manufacturer
- BABYFACE LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 36d6141c-6967-d779-e063-6294a90af0a7
- SPL ID
- 4616746b-6ba3-79eb-e063-6394a90ab18a
- Version
- 2
- Effective date
- 2025-12-16
- Source export date
- 2026-10-30
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/8d15bdc5962e7531569eaeb5b1b2e4919574d40a6782ab67345a27b890175a00/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:58:51
| 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 | Non Tinted Mineral Sunscreen | openfda.brand_name | |
| generic name | TITANIUM DIOXIDE, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | BABYFACE LLC | openfda.manufacturer_name | |
| ndc | package | 85374-202-50 | openfda.package_ndc |
| ndc | product | 85374-202 | openfda.product_ndc |
| ndc11 | package | 85374020250 | derived:openfda.package_ndc |
| spl id | 4616746b-6ba3-79eb-e063-6394a90ab18a | id | |
| spl set id | 36d6141c-6967-d779-e063-6294a90af0a7 | 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.