FDA.reportPublic FDA data

SUN CONTROL BROAD SPECTRUM 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
SUN CONTROL BROAD SPECTRUM SPF 30
Generic name
HOMOSALATE, OCTISALATE, ZINC OXIDE
Manufacturer
SKINPLAN.US LLC
Product type
HUMAN OTC DRUG
SPL set ID
8e34a343-7253-469f-9973-076a7ae26cbc
SPL ID
161fc0cf-491c-2123-e063-6294a90aaa7a
Version
1
Effective date
2024-04-15
Source export date
2026-08-01
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/29baabee7fa6726d72190670d84f1571113181a958a8119cbe97e8f0d1d955b2/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:13:30
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 or irritation develops and last. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away If pregnant or breast-feeding, ask a health professional before use.