FDA label b573d62a-a156-49dc-8dcb-d96ccb9ae3e1

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
2e0bcab3-829d-45e4-96b3-0f97378b5fc5
SPL ID
b573d62a-a156-49dc-8dcb-d96ccb9ae3e1
Version
2
Effective date
2017-12-05
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:05:28

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 For external use only Discontinue use and consult a Physician if a rash or other adverse reaction occurs, or if symptoms worsen or persist for more than 7 days Children under 12 – Ask your doctor Avoid contact with eyes or mucus membranes If Pregnant or breast feeding, ask a physician before use Do not use with other topical products Do not use on open wounds If swallowed, seek professional help and contact Poison Control immediately

Reported adverse events (FAERS/openFDA)#

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