FDA label a2df68dd-3330-6f24-e053-2995a90a011c

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
f498fec9-92e5-4719-927e-1de5f4dfdc61
SPL ID
a2df68dd-3330-6f24-e053-2995a90a011c
Version
1
Effective date
2020-04-09
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:06

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

Warnings For external use only When using this product do not use in or near the eyes. If contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation develops and persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Directions For use apply thoroughly to hands as desired. Allow to dry without wiping. Discard wipe in trash receptacle after use. Do not flush. For dispensing peel back front label at tab. Remove towelettes as needed. Reseal pouch by pressing label firmly back into place.

Reported adverse events (FAERS/openFDA)#

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