Native Mineral Suncare Zinc Oxide Sunscreen Unscented Broad Spectrum 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 (canonical bytes are SHA-256 checked before publication)

Brand name
Native Mineral Suncare Zinc Oxide Sunscreen Unscented Broad Spectrum SPF 30
Generic name
ZINC OXIDE
Manufacturer
The Procter & Gamble Manufacturing Company
Product type
HUMAN OTC DRUG
SPL set ID
447347d6-b8a3-7338-e063-6294a90abbf9
SPL ID
447348f2-6efd-a1cd-e063-6394a90a3cce
Version
1
Effective date
2025-11-25
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:05:25
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. keep away from face to avoid breathing it. Stop use and ask a doctor if rash occurs Keep out of reach of children. If product is swallowed, get medical help, or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.