warnings
Baby Bare Republic Mineral Sunscreen Warning Label
Baby Bare Republic 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
- Baby Bare Republic Mineral Sunscreen
- Generic name
- ZINC OXIDE
- Manufacturer
- COOLA, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b292d1a9-7ff8-0faf-e053-2995a90ae342
- SPL ID
- 43915b65-3d50-2fb7-e063-6294a90a3275
- Version
- 6
- Effective date
- 2025-11-14
- Source export date
- 2026-10-30
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/a900515c00f4d0d29f88cc94ee68daf127f036296f87a6b4a8a3f964cd0433c0/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:49:49
| 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 | Baby Bare Republic Mineral Sunscreen | openfda.brand_name | |
| generic name | ZINC OXIDE | openfda.generic_name | |
| manufacturer name | COOLA, LLC | openfda.manufacturer_name | |
| ndc | package | 79753-007-01 | openfda.package_ndc |
| ndc | product | 79753-007 | openfda.product_ndc |
| ndc11 | package | 79753000701 | derived:openfda.package_ndc |
| spl id | 43915b65-3d50-2fb7-e063-6294a90a3275 | id | |
| spl set id | b292d1a9-7ff8-0faf-e053-2995a90ae342 | set_id | |
| unii | SOI2LOH54Z | 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.