Florida Glow 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
Florida Glow SPF 30
Generic name
AVOBENZONE,OCTOCRYLENE,OCTISALATE,HOMOSALATE
Manufacturer
Southeast Holdings Corp.
Product type
HUMAN OTC DRUG
SPL set ID
20538bc0-10c3-492c-952a-6797e46003f2
SPL ID
436d52df-1e06-52c8-e063-6394a90a368a
Version
3
Effective date
2025-11-12
Source export date
2026-09-28
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:40:44
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. Stop use and ask a doctor if rash occurs. Do not use on damaged or broken skin. When using this product Keep out of eyes.Rinse with water to remove. Keep out of reach of children . If product is swallowed, get medical he$ or contact a Po1son Control Center right away.

Reported adverse events (FAERS/openFDA)#

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