FDA label d3660ce8-8dfa-4bbf-aba6-49b89803c5d1

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
dd563ee5-d317-4bef-8faa-3e178ee1c998
SPL ID
d3660ce8-8dfa-4bbf-aba6-49b89803c5d1
Version
2
Effective date
2019-12-05
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:12:42

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

WARNINGS Warnings: 1.For external use only 2. Stop using of this product if any below symptom is found. Continuous use may worsen this symptom. Please contact dermatologist. a) In case of any trouble, such as red spots, swollen skin, itchy or irritation. b) In case of any trouble on applied area as above due to direct light. 3. Do not use on wounded areas. 4. Keeping Caution a) Please keep away from children. b) Do not keep in direct light area.

Reported adverse events (FAERS/openFDA)#

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