FDA label 6f32b549-4797-0610-e053-2a91aa0a415c

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)

SPL set ID
6f32051a-944a-686e-e053-2991aa0aebd1
SPL ID
6f32b549-4797-0610-e053-2a91aa0a415c
Version
2
Effective date
2018-06-21
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:04

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

1. Discontinue use and ask a doctor if any adverse reactions occur such as rash, swelling or irritation after use or due to direct sunlight. 2. Do not use on damaged or broken skin. 3. Storage and Handling Precautions (A)Keep out of reach of children. (B)Keep out of direct sunlight. 4. Avoid contact with eyes. If there is any problem with this product, compensation is offered by based on ‘Consumer Dispute Resolution Criteria’, notice by The Fair Trade Commission. Customer Support Center +82-2-512-0478

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.