FDA label d59a4036-ddeb-f174-e053-2995a90a4bec

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
a57d2008-f8f1-9de0-e053-2a95a90a4828
SPL ID
d59a4036-ddeb-f174-e053-2995a90a4bec
Version
4
Effective date
2022-01-15
Source export date
2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:45:06

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

Warning For external use only. Do not use ■in or contact the eyes. When using this product ■These wipes do not replace wipes used for medical procedures. these wipes are meant for general cleansing. ■Keep in a dry place away from fire. ■Discontinue use if iritation and redness develop. If the condition persists for more than 72 hours, consult a physician. ■Please close the lid after dispensing to maintain purity. Alcohol by nature evaporates quickly. ■Store below 95°F (35°C). Keep this out of reach of children.f swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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