Home FDA labels 55006247-4bd3-0b27-e063-6394a90aef16 Euthymol Whitening Purple Corrector 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 Euthymol Whitening Purple Corrector
Generic name SODIUM FLUORIDE
Manufacturer LG HOUSEHOLD & HEALTH CARE LTD.
Product type HUMAN OTC DRUG
SPL set ID 5500686c-d417-c50a-e063-6294a90ac7fa
SPL ID 55006247-4bd3-0b27-e063-6394a90aef16
Version 3
Effective date 2026-06-24
Source export date 2026-11-06
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/2026-11-06/b433ab6a44616055e476a7876dbdd70a7f81f656e17ee28dc50dad20e67316bd/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run 20261106T075659Z
Imported at 2026-11-06 09:26:04 Harmonized routes table Harmonized routes DENTAL
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 . Keep out of reach of children Keep out of reach of children under 6 years of age. Do not Do not swallow. If you accidentally swallow more than used for brushing, seek professional assistance or contact a poison control center right away. If an allergic reaction develops, discontinue use immediately.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.