FDA label d64d0373-59ac-6b59-e053-2995a90a0ff6

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
b4c024ef-1dfa-41f1-e053-2995a90a4625
SPL ID
d64d0373-59ac-6b59-e053-2995a90a0ff6
Version
5
Effective date
2022-01-23
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:21:13

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

DO NOT SORE ABOVE 105 F MAY DISCOLOR SOME FABRICS. HARMFULA TO WOOD FINISHES AND PLASTICS. FOR HANDS ESTERNAL USE ONLY. FLAMMABLE , KEEP AWAY FROM FIRE OR FLAME WHEN USING THIS PRODUCT KEEP OUT OF EYES, IN CASE OF CONTACT WITH EYES FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN. DO NOT INHALE OR INGEST. STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS OR IF CONDITION PERSISTS FOR MORE THEN 72 HOURS.

Reported adverse events (FAERS/openFDA)#

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