FDA label 2f09a0fc-467f-4bba-84eb-e62f0bc55158

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
d2b295d2-9fdb-449b-89b3-16be29b077de
SPL ID
2f09a0fc-467f-4bba-84eb-e62f0bc55158
Version
1
Effective date
2018-12-17
Source export date
2026-11-06
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/2026-11-06/5ab46f90f6b44e2aa9affb3cb9a1420d82b92a8f942c23fe463364760a659d66/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:10:18

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 ony as directed. do not bandage tightly or use witha heating pad. avoid contact with eyes or mucous membranes. do not apply to wounds or damages skin. avoid sun exposure to area applied. Stop use and ask a doctor if- condition worsens. smptoms persist for more than 7 dayd or clear up and occur again within a few days. severe skin irritation occurs or allergic reaction develops. If pregnant or breast-feeding, ask a healthcare professional before use. Nursing mothers should not apply to breast area. Keep out of reac of children. If swallowed, b 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.