FDA label b3d53430-700f-4f1f-e053-2a95a90aafdc

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
c5d1eb0d-d1d8-4ec7-968e-b9774bb88108
SPL ID
b3d53430-700f-4f1f-e053-2a95a90aafdc
Version
3
Effective date
2020-11-11
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:30:00

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.