ACTIDOSE

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)

Brand name: ACTIDOSE
Generic name: ACTIVATED CHARCOAL
Manufacturer: Padagis US LLC
Product type: HUMAN OTC DRUG
SPL set ID: 76e4fe6a-afd4-4f68-b12d-0b094f750615
SPL ID: cf3da077-fe7d-4685-8c5c-f773bc88c88d
Version: 8
Effective date: 2026-07-28
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 01:39:39

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M023	openfda.application_number
brand name		ACTIDOSE	openfda.brand_name
generic name		ACTIVATED CHARCOAL	openfda.generic_name
manufacturer name		Padagis US LLC	openfda.manufacturer_name
ndc	package	0574-0520-76	openfda.package_ndc
ndc	package	0574-0520-74	openfda.package_ndc
ndc	product	0574-0520	openfda.product_ndc
ndc11	package	00574052074	derived:openfda.package_ndc
ndc11	package	00574052076	derived:openfda.package_ndc
rxcui		1251411	openfda.rxcui
rxcui		309150	openfda.rxcui
spl id		cf3da077-fe7d-4685-8c5c-f773bc88c88d	id
spl set id		76e4fe6a-afd4-4f68-b12d-0b094f750615	set_id
unii		2P3VWU3H10	openfda.unii

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 give activated charcoal until after the 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.

Reported adverse events (FAERS/openFDA)#

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