FDA label d3bf4f1b-551c-0045-e053-2a95a90a8c09

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
ce8bd6c1-cbf2-4c18-909c-65ca2343d30f
SPL ID
d3bf4f1b-551c-0045-e053-2a95a90a8c09
Version
4
Effective date
2021-12-22
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:13:37

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 and mucous membranes -If condition worsens or if symptoms persist for more than 7 days or clear up and appear again within a few days, discontinue use of this product and consult a doctor. -When used for arthritis, if pain persists for more than 10 days or redness is present or in conditions affecting children under 12 years of age, consult a physician immediately.

Reported adverse events (FAERS/openFDA)#

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