FDA label 60933f5f-5886-4408-ba4d-5c69ad6f2acb

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
4023f02b-d453-4f13-ba98-4964fb7461ed
SPL ID
60933f5f-5886-4408-ba4d-5c69ad6f2acb
Version
9
Effective date
2015-07-08
Source export date
2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:33:40

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 and cautions

Warnings For external use only Avoid contact with eyes Do not applly to open wounds or damaged skin If symptoms persist for more than seven days, discontinue use and consult physician If swallowed, consult physician Do not bandage tightly If pregnant or breast feeding, contact physician prior to use Do not use in large quantities, particularly over raw surfaces or blistered areas

Reported adverse events (FAERS/openFDA)#

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