Sun Shield Body Glow SPF50

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
Sun Shield Body Glow SPF50
Generic name
HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Manufacturer
Koco Life LLC
Product type
HUMAN OTC DRUG
SPL set ID
180aa4d5-6dac-e658-e063-6394a90a3287
SPL ID
180aa4d5-6dad-e658-e063-6394a90a3287
Version
1
Effective date
2024-06-28
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:27:55
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 • 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 • Stop use and ask a doctor if rash occurs • Keep out of reach of children • If product is swallowed, get medical help orcontact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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