FDA label 1134f978-a279-46e7-9bef-9fd648fa89a9

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
70392efa-5b3e-4b5b-81bb-3d1b4e7db955
SPL ID
1134f978-a279-46e7-9bef-9fd648fa89a9
Version
1
Effective date
2014-03-21
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 06:11:41

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. Do not swallow. Avoid contact with eyes. If contacted, flush eyes with water. Should a rash or irritation develops, discontinue use. If condition worsens, or if symptoms persist for more than 7 days, consult a physician. Do not use in large quantities, particularly over raw surfaces or blistered areas. Keep out of the reach of children.

Reported adverse events (FAERS/openFDA)#

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