FDA label 2117e613-56b4-401b-b2bf-b37b0b750dfe

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
307738ec-fe53-48e5-9ba2-0ec2c23e8a82
SPL ID
2117e613-56b4-401b-b2bf-b37b0b750dfe
Version
4
Effective date
2021-03-17
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:42:08

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. using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin, if this occurs, only one medication should be used unless directed by a doctor. do not get into eyes, if excessive skin irritation develops or increases, discontinue use and consult a doctor. apply to affected areas only.

Reported adverse events (FAERS/openFDA)#

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