Home FDA labels 47ed1b50-7ba6-110e-e063-6394a90a0559 Dr.Jart Premium Beauty Balm Light Medium-Medium 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 Dr.Jart Premium Beauty Balm Light Medium-Medium
Generic name ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
Manufacturer Have & Be Co., Ltd.
Product type HUMAN OTC DRUG
SPL set ID 45b1c2c6-a45b-4a45-bec9-e5341079c0a1
SPL ID 47ed1b50-7ba6-110e-e063-6394a90a0559
Version 5
Effective date 2025-12-31
Source export date 2026-09-28
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/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:40:38 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 · 13 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 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. Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away. Stop using and ask a doctor if rash occurs.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.