FDA label dc2480d4-700f-7054-e053-2a95a90a97b5

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
eb7d8270-1596-411a-bfaf-bb03b7ca6f70
SPL ID
dc2480d4-700f-7054-e053-2a95a90a97b5
Version
4
Effective date
2022-04-08
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:33

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. • Avoid contact with eyes or mucous membranes. • If symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. • If swallowed, contact physician or Poison Control center. • Do not apply to wounds a damaged skin. • Do not bandage tightly or use with a heating pad. Do not use if pregnant or breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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