Home FDA labels 358399ee-bc12-06a1-e063-6394a90a9d96 EUTHYMOL WHITENING SET 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 SET
Generic name SODIUM FLUORIDE
Manufacturer LG HOUSEHOLD & HEALTH CARE LTD.
Product type HUMAN OTC DRUG
SPL set ID 35839b10-4c40-40e5-e063-6294a90a85b4
SPL ID 358399ee-bc12-06a1-e063-6394a90a9d96
Version 3
Effective date 2025-05-19
Source export date 2026-11-06
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/3b52cde3709f43d454872fcaffdb78395b270bc65272c06ef1005cc77c998864/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run 20261106T075659Z
Imported at 2026-11-06 09:01:14 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 · 18 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 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.