Home FDA labels 7f1bf75c-5f3e-42c2-a2d0-d7a5877f0309 LUMINOUS EYE CORRECTOR SPF 41 - TAN 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 LUMINOUS EYE CORRECTOR SPF 41 - TAN
Generic name TITANIUM DIOXIDE, ZINC OXIDE
Manufacturer Drmtlgy, LLC
Product type HUMAN OTC DRUG
SPL set ID 5c5aad09-9f93-4634-8db1-c67570b38b2b
SPL ID 7f1bf75c-5f3e-42c2-a2d0-d7a5877f0309
Version 4
Effective date 2026-05-04
Source export date 2026-10-30
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/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run 20261102T182004Z
Imported at 2026-11-02 19:44:06 Harmonized routes table Harmonized routes TOPICAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 11 matching rows.
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 swallowed, get medical help or contact a Poison Control Center right away.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.