FDA label 6ea2d37f-979d-4d61-89ec-9f1c6f26ecfd

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
56994b77-e7e1-402a-a3f6-5591bf86d963
SPL ID
6ea2d37f-979d-4d61-89ec-9f1c6f26ecfd
Version
3
Effective date
2018-03-27
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:46

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 Use only as directed Avoid contact with eyes and mucous membranes Do no apply to wounds or damaged skin Do not bandage tightly or use a heating pad Stop use and ask doctor if Excessive redness or irritation is present Condition worsens Pain persists for more than 7 days Symptoms clear up and occur again within a few days If pregnant of breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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