FDA label f8376280-0476-4dfd-8be8-64312266def0

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
71197538-9317-43cb-a370-85277ee5889f
SPL ID
f8376280-0476-4dfd-8be8-64312266def0
Version
7
Effective date
2010-08-17
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 05:51:06

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. Use only as directed. Keep out of reach of children to avoid accidental poisoning. avoid contact with eyes or mucous membranes. discontinue use if excessive irritation of the skin develops. do not bandage tightly, apply to wounds, or damaged skin, or use with a heating pad if condition worsens, or if symptoms persist for more than 7 days or clear-up and occur again within a few days, consult a doctor if skin redness or irritation develops, discontinue use of this product and consult a doctor. 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.