FDA label 60e29ef6-0b0a-559a-e053-2a91aa0a5cb0

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
6e0cd3a0-6b4d-4469-bb18-083cb1d7887a
SPL ID
60e29ef6-0b0a-559a-e053-2a91aa0a5cb0
Version
3
Effective date
2017-12-21
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:43

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 Do not use if you have A know allergy or sensitivity to any of the ingredients. Have a history of severe liver disease or impairment When using this product You may not have pain - Avoid sources of heat or injury You may have burning or stinging if accidental eye contact You mat have temporary skin irritation or sensitivity Keep out of eyes and mouth. Keep out of reach of children. Do not use if pregnant or breast feeding. If accidentally swallowed get medical help right away. Not for chronic use.

Reported adverse events (FAERS/openFDA)#

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