FDA.reportPublic FDA data

SUNSCREEN BROAD SPECTRUM SPF 50 FACE AND BODY

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
SUNSCREEN BROAD SPECTRUM SPF 50 FACE AND BODY
Generic name
AVOBENZONE/OCTISALATE/OCTOCRYLENE
Manufacturer
Mary Kay Inc.
Product type
HUMAN OTC DRUG
SPL set ID
2c4eaf2e-b034-8185-e063-6394a90a8275
SPL ID
2c4eaf2e-b035-8185-e063-6394a90a8275
Version
1
Effective date
2025-01-22
Source export date
2026-08-01
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/206e0852f7011b53c21719ec5c68ac6752381d0fcd1d348f7428adad64429e89/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:19:42
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 Do not use on broken skin. When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.