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
2026-10-12
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/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:12:53
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

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.