FDA.reportPublic FDA data

FDA label a72db80d-7e6d-4d8c-8cfa-43ddab8cee31

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
9a341bb0-db8e-4100-a609-45dfc4ffce6a
SPL ID
a72db80d-7e6d-4d8c-8cfa-43ddab8cee31
Version
2
Effective date
2023-04-25
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:40:55

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 ∙ avoid contact with eyes and mucous membranes ∙ do not apply to wounds or damaged skin ∙ do not bandage tightly or use with a heating pad ■ Stop use and ask doctor if ∙ condition worsens ∙ symptoms persist for more than 7 days or clear up and occur again within a few days ■ Keep out of reach of children. If swallowed, get medical help or contact a Poison control Center immediately. ■ If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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