FDA label 11460960-daf6-e8b7-e063-6394a90a9b31

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
404cd08d-d4bd-447e-a284-bc0499cbc0fb
SPL ID
11460960-daf6-e8b7-e063-6394a90a9b31
Version
7
Effective date
2024-02-13
Source export date
2026-11-06
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:04:45

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 If pregnant or breastfeeding consult a healthcare professional before use. Do not use on children 2 years of age unless directed by a doctor. When using this product avoid contact with eyes Use only as directed by a doctor on persons with highly sensitive skin. Stop use and consult a doctor if there is no improvement within 4 weeks irritation occurs Keep out of children. If accidental ingestion occurs, 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.