FDA label 55fd49ea-635d-41e4-b557-83fb894b200b

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
8d3a45e3-f1a3-43c0-9529-86353bf582f7
SPL ID
55fd49ea-635d-41e4-b557-83fb894b200b
Version
1
Effective date
2011-11-28
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:00

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. Keep out of reach of children. Avoid eye area, if eye contact occurs, flush gently and thoroughly with water. Discontinue use if rash or irritation occurs. If irritation persists, consult your health care practitioner. Within the USA Call 888-215-3891 DrEvans.com Guthy-Renker ® , LLC P.O. Box 14383, Palm Desert, CA 92555-4383, London UK SW1Y 4HH, Sydney, Australia 2138, Auckland, New Zealand, Toronto, Ontario M1X 1E7 Dr. Evans is a registered trademark of TEC Production Corporation Evans/Syal DR. E tm

Reported adverse events (FAERS/openFDA)#

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