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FDA label 8b19f3e8-5b30-4f77-9484-3544dadfad18

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
b0854d7b-24bc-4d65-bf59-6716b5f999b5
SPL ID
8b19f3e8-5b30-4f77-9484-3544dadfad18
Version
3
Effective date
2025-09-17
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:40:24

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 Activated Charcoal until after patient has vomited unless directed by a health professional. Do not use in persons who are not fully conscious. Do not use this product unless directed by a health professional if turpentine, corrosives such as alkalies (lye) and strong acids or petroleum distillates, such as kerosene, gasoline, paint thinner, cleaning fluid or furniture polish have been ingested. Do not use if poison victim is unconscious or having convulsions. Keep patient active and moving.

Reported adverse events (FAERS/openFDA)#

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