FDA label 7cf01a53-2d9c-5012-e053-2a91aa0ac1fe

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
597f533e-077f-48b8-b4ba-2ed640fb897c
SPL ID
7cf01a53-2d9c-5012-e053-2a91aa0ac1fe
Version
2
Effective date
2018-12-13
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:34:27

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

FOR EXTERNAL USE ONLY, KEEP OUT OF REACH OF CHILDREN, FLAMMABLE, KEEP AWAY FROM OPEN FLAME AND SOURCES OF HEAT. AVOID CONTACT WITH EYES SHOULD THIS OCCUR FLUSH EYES WITH WATER. IF IRRITATION DEVELOPS, DISCONTINUE USE AND CONTACT A PHYSICIAN. IF SWALLOWED, CONTACT A PHYSICIAN. DO NOT STORE ABOVE 40 ​0 ​C/110 ​0 ​F

Reported adverse events (FAERS/openFDA)#

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