FDA label f183f9bf-558b-4a99-e053-2995a90a0878

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
d7e394b6-3e88-445b-82eb-3b89d70eb8b3
SPL ID
f183f9bf-558b-4a99-e053-2995a90a0878
Version
1
Effective date
2023-01-05
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:15:55

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. When using this product Avoid contact with eyes. Do not apply to wounds or damaged, broken or irritated skin Stop use and ask a doctor If • Condition worsens. • Irritation develops. Redness appears. • Symptoms persist for more than 7 days or clear up and occurs again within a few days. Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center right away. Emergency Number : 1-800-222-1222 IF PREGNANT OR BREASTFEEDING , ask a heath professional before use

Reported adverse events (FAERS/openFDA)#

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