FDA.reportPublic FDA data

FDA label cab51b1d-a07b-4249-a146-bde1ddb992da

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
89a22711-a05c-41a0-a0c3-4faa3eb43741
SPL ID
cab51b1d-a07b-4249-a146-bde1ddb992da
Version
1
Effective date
2014-03-15
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:20:54

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. if you have any abnormal symptoms as followings, you should discontinue to use this cream. In case of using continuously, you have to consult to dermatologist because it may make symptoms worse. a. red macule, swelling, urtication, and irritation during use b. symptoms like above by direct ray 2. do not use if you have a wound, eczema, and dermatitis to the area where you apply this cream 3. caution during storing and handling a. close the cap after use b. keep it to the area where babies and infants cannot reachto c. keep it to the area where has not high or low temperature and has no direct ray

Reported adverse events (FAERS/openFDA)#

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