FDA label c13590c9-130e-733a-e053-2a95a90a77d7

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
c4e5ab20-cd2f-42ad-bbfe-bf0dbedf6dd0
SPL ID
c13590c9-130e-733a-e053-2a95a90a77d7
Version
3
Effective date
2021-04-30
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:28

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 fire & flame Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances When using this product Avoid the eyes and mucous membranes In the case of eyes or mucous membrane contact, rinse area thoroughly with water Stop use and ask a doctor if Condition worsens Redness or irritation develops Condition persist 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.