FDA label bd74663b-18ea-47c4-9135-cd8573d8f246

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
4b9dfe7e-ccd1-4115-bc06-07e63eee4712
SPL ID
bd74663b-18ea-47c4-9135-cd8573d8f246
Version
3
Effective date
2018-03-23
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:14:05

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 on broken skin. If symptoms persist or worsen, discontinue use and seek medical attention. Avoid contact with eyes. If product gets into eyes, flush with water and seek medical attention. If an allergic reaction occurs, discontinue use and seek medical attention. If rash, redness, irritation, or itching occurs, discontinue use. If pregnant or breastfeeding, ask a health professional before use. If swallowed, get medical help or contact a Poison Control Center right away. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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