FDA.reportPublic FDA data

FDA label ac267861-16f1-7537-e053-2995a90a2d09

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
ac265ea1-e71c-f149-e053-2995a90ac30a
SPL ID
ac267861-16f1-7537-e053-2995a90a2d09
Version
1
Effective date
2020-10-21
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:23:20

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

For external use only. Avoid contact with eyes, mucous membranes, damaged skin, or wounds. Do not use if you are allergic to any of this product's active or inactive ingredients. If pregnant or breast-feeding, ask a health professional before use. Stop use and ask a doctor if symptoms worsen or persist for more than 3 days. Discontinue treatment in case of skin irritation, redness or rash occurs. If swallowed , get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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