ACTIDOSE AQUA

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 AQUA
Generic name: ACTIVATED CHARCOAL
Manufacturer: Padagis US LLC
Product type: HUMAN OTC DRUG
SPL set ID: c85dc235-3f42-4361-9bd2-1aaff798ad75
SPL ID: bd250d66-b8ea-4cab-a8f2-d2913a157fc5
Version: 9
Effective date: 2026-07-28
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:41:22

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M023	openfda.application_number
brand name		ACTIDOSE AQUA	openfda.brand_name
generic name		ACTIVATED CHARCOAL	openfda.generic_name
manufacturer name		Padagis US LLC	openfda.manufacturer_name
ndc	package	0574-0521-25	openfda.package_ndc
ndc	package	0574-0521-76	openfda.package_ndc
ndc	package	0574-0521-74	openfda.package_ndc
ndc	product	0574-0521	openfda.product_ndc
ndc11	package	00574052174	derived:openfda.package_ndc
ndc11	package	00574052125	derived:openfda.package_ndc
ndc11	package	00574052176	derived:openfda.package_ndc
rxcui		1251411	openfda.rxcui
rxcui		309150	openfda.rxcui
spl id		bd250d66-b8ea-4cab-a8f2-d2913a157fc5	id
spl set id		c85dc235-3f42-4361-9bd2-1aaff798ad75	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.