FDA label f34ca0c5-5ee4-4b91-ba8c-ba8e54ce3727

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
cfd83ed1-0a3f-4747-9efe-9b15e13eae12
SPL ID
f34ca0c5-5ee4-4b91-ba8c-ba8e54ce3727
Version
1
Effective date
2020-06-15
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:23:46

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 you are allergic to any of the ingredients When using this products Avoid contact with eyes. in case of contact, rinse eyes thoroughly with water. Avoid contact with broken, irritate. or itching skin. Stop use and ask a doctor if irritation or redness develops and condition persists for more than 72 hours. Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center(1-800-222-1222) right away. If pregnant or brest-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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