EIGHT SAINTS Chase The Sun 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
EIGHT SAINTS Chase The Sun SPF-30
Generic name
OCTOCRYLENE, OCTISALATE, ZINC OXIDE
Manufacturer
BRICKELL BRANDS LLC
Product type
HUMAN OTC DRUG
SPL set ID
9b19b2b4-d8b9-415d-a217-4a5ef3d75a8c
SPL ID
09e3156c-9351-43f6-e063-6394a90ad71e
Version
2
Effective date
2023-11-11
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:15:20
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

Warnings: • External use only. Do not use • on damaged or broken skin. When using this product • keep out of eyes. Rinse with water to remove. Stop use and ask a doctor • if irritation or rash develops. Keep out of reach of children. • If product is swallowed, get medical attention or contact poison control center immediately. If pregnant or breast-feeding, • ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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