Home FDA labels 4f0be9a2-5641-baaf-e063-6394a90a0f5b Arizona Sun Sunscreen SPF 8 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 Arizona Sun Sunscreen SPF 8
Generic name SUNSCREEN
Manufacturer Arizona Sun Products
Product type HUMAN OTC DRUG
SPL set ID 11e8b612-29be-47ed-e063-6394a90ab9e7
SPL ID 4f0be9a2-5641-baaf-e063-6394a90a0f5b
Version 2
Effective date 2026-04-09
Source export date 2026-10-30
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run 20261102T182004Z
Imported at 2026-11-02 19:20:09 Harmonized routes table 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.
Harmonized identifiers page 1 of 1 · 13 matching rows.
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 Warnings For external use only. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if if rash or irritation develops and lasts. Keep out of the reach of children. If 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.