FDA.reportPublic FDA data

5281 SUNSCREEN

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
5281 SUNSCREEN
Generic name
AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE
Manufacturer
Innovation Specialties
Product type
HUMAN OTC DRUG
SPL set ID
86fc4539-e1c5-4d0f-a418-f48729cb2b20
SPL ID
1cee97c2-00a1-c8b8-e063-6294a90ac4c6
Version
3
Effective date
2024-07-10
Source export date
2026-08-01
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/2026-08-01/a02fd54f2831abedf72de26b709069bc80ecbb9303a4823ffe5695ea1bb3d85a/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:40:13
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 swallowed, get medical help or contact a Poison Control Center right away.