FDA label 589803b1-7e58-4e60-9ac5-b17fe07d0474

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
2ac1f9bb-2766-47eb-b25d-ac70f671a309
SPL ID
589803b1-7e58-4e60-9ac5-b17fe07d0474
Version
1
Effective date
2012-03-28
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:40

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. If swallowed, get medical help or contact a Poison Control Center immediately. Keep out of the reach of children. STOP USE AND ASK A DOCTOR IF: Conditions worsen or clear up and then recur The condition persists for more than 7 days A rash or allergic reaction occurs DO NOT USE: In the eyes Over large areas of the body If you are allergic to any of the ingredients Longer than 1 week unless directed by a doctor On raw surfaces, blistered areas or serious burns For deep lacerations or puncture wounds WHEN USING THIS PRODUCT: Avoid contact with the eyes or mucus membranes

Reported adverse events (FAERS/openFDA)#

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