FDA label d18f8736-a106-4e7f-a303-790e5bdbede2

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
a9f9d381-64d7-4de5-b59d-af5554e81259
SPL ID
d18f8736-a106-4e7f-a303-790e5bdbede2
Version
1
Effective date
2018-01-02
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:29:36

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 Warnings: For external use only 1. Discontinue use immediately and consult a dermatologist, if you experience the following: 1) Irritation, red spot, itchy skin or rash 2) Applied skin area has the above reaction from direct sun. 2. Do not use on irritated skin, cuts, or other infected skin areas. 3. Avoid direct contact with eyes

Reported adverse events (FAERS/openFDA)#

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