FDA label 4721af1e-127e-22c3-e063-6394a90a6d47

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
c473d34f-7d78-4a66-ac91-a25bb46dbd1c
SPL ID
4721af1e-127e-22c3-e063-6394a90a6d47
Version
3
Effective date
2025-12-29
Source export date
2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:43:09

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 . Do not use if tube foil seal is broken or missing. Do not use on broken skin. When using this product , avoid contact with eyes; if contact occurs, rinse abundantly with water to remove. Stop use and ask a doctor - if symptoms persist for more than 3 days or worsen - if hypersensitivity and/or allergy occurs. Keep out of reach of children . If ingested, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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