FDA label 2b8df770-78db-42a0-e063-6394a90ac30d

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
9e79b3a5-d59b-4ceb-8f89-5d0f8101b1d4
SPL ID
2b8df770-78db-42a0-e063-6394a90ac30d
Version
2
Effective date
2025-01-12
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:48:17

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

Warning For external use only. Stop use and ask a doctor if Hypersensitivity symptoms suchas erythema, itching and dermatitis happen. Skin irritation happens. If dollowing avnomal symptoms persist, discontinue use irritation around the eyes, ears mucous membranes, including the mouth, under the skin irritation and rashes. Other Information: Read the directions and warning before use Avoid freezing and excessive heat above 40℃ (104℉). ●If swallowed, get medical help or contact a Poison Contrl Center right away.

Reported adverse events (FAERS/openFDA)#

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