FDA label 086c92a9-2e28-a240-e063-6394a90a5089

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
c134d931-fda7-8fd9-e053-2a95a90abecf
SPL ID
086c92a9-2e28-a240-e063-6394a90a5089
Version
3
Effective date
2023-10-23
Source export date
2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:04:08

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. Flammable, keep away from heat and flame Does not contain grain alcohol; do not drink. If taken internally will produce serious gastric disturbances When using this product Avoid the eyes and mucous membranes In the case of eyes or mucous membrane contact, rinse thoroughly with water Stop use and ask a doctor if Condition worsens Redness or irritation develops If condition persists for more than 3 days Keep out of reach of children. If swallowed contact a doctor or Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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