Activated charcoal


Activated charcoal
Accession Number
DB09278  (DB05269)
Small Molecule

Activated charcoal, or activated carbon, is an amorphous form of carbon prepared from incomplete combustion of carbonaceous organic matter. It is activated by an oxidizing gas flow at high temperature passed over its surface to make a fine network of pores, producing a material with large surface area and high affinity for various substances. It is used as a gastric decontaminant and emergency medication to treat poisonings following excessive oral ingestion of certain medications or poisons by absorbing most drugs and toxins. However its effects is rendered poor on some compounds including strong acids or bases, methanol and substances with limited absorptive capacity (including iron, lithium, arsenic). It works by binding to the poison in the gastric contents in a reversible fashion thus may be adminstered together with a cathartic to reduce the small intestine transit time. The clinical applications of activated charcoal occured in the early 1800's. While this management for acute poisoning is considered fairly invasive, it is on the World Health Organization's List of Essential Medicines that includes the most important medications needed in a basic health system.

  • Activated carbon
  • Carbo activates
  • Carbo activatus
  • Carbo vegetabilis
  • Carbon
  • Carbón activado
  • Carbon, Activated
  • Carbon, decolorizing
  • carbono
  • Charcoal activated
  • Charcoal-activated
  • Charcoal, Activated
  • Charcoal,activated
  • Medicinal carbon
  • Medicinal charcoal
External IDs
AST 120 / AST-120 / GC BM-3
Prescription Products
NameDosageStrengthRouteLabellerMarketing StartMarketing End
ActidoseSuspension208 mg/1mLOralPaddock Laboratories, LLC1983-10-01Not applicableUs
Actidose AquaSuspension208 mg/1mLOralPaddock Laboratories, LLC1984-01-01Not applicableUs
Activated CharcoalSuspension208 mg/1mLOralHF Acquisition Co LLC, DBA HealthFirst2018-12-22Not applicableUs
Char-flo Aqueous Base - Sus Orl 208mg/mlSuspensionOralBallard Medical Products1997-08-202004-08-04Canada
Charcodote-aqueous Sus 200mg/mlSuspensionOralPharmascience Inc1997-03-172019-01-17Canada
Additional Data Available
  • Application Number
    Application Number

    A unique ID assigned by the FDA when a product is submitted for approval by the labeller.

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  • Product Code
    Product Code

    A governmentally-recognized ID which uniquely identifies the product within its regulatory market.

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Over the Counter Products
NameDosageStrengthRouteLabellerMarketing StartMarketing End
Activated CharcoalCapsule225 mgOralJamp Pharma CorporationNot applicableNot applicableCanada
Activated CharcoalCapsuleOralLaboratoire Leo Desilets M.H. Inc1998-10-07Not applicableCanada
Activated Charcoal 260mgCapsuleOralExzell Pharma Inc1998-12-07Not applicableCanada
Activated Charcoal Cap 280mgCapsuleOralNutrition Professionals Inc.1988-12-311997-02-27Canada
Activated Charcoal Cap 280mgCapsuleOralNature's Way Of Canada Ltd.1984-12-312010-07-27Canada
Activated Charcoal PowderPowder, for solutionOralLaboratoire Leo Desilets M.H. Inc1999-04-082013-06-18Canada
Activated Charcoal USPPowderOralLifeforce Nutri Blends Canada Inc.2002-06-172012-07-05Canada
Adrien Gagnon Charbon Activé/activated Charcoal CapsulesCapsuleOralSantÉ Naturelle (Ag) LtÉe2009-12-212014-06-09Canada
Biochala Charbon Activé/activated CharcoalCapsuleOralImportations Biochala Inc.Not applicableNot applicableCanada
Charac-25SuspensionOralOmega Laboratories Ltd1985-12-31Not applicableCanada
Additional Data Available
  • Application Number
    Application Number

    A unique ID assigned by the FDA when a product is submitted for approval by the labeller.

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  • Product Code
    Product Code

    A governmentally-recognized ID which uniquely identifies the product within its regulatory market.

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Mixture Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing End
CarbosylaneActivated charcoal (140 mg) + Dimethicone (45 mg)CapsuleOralLaboratoires Grimberg1990-12-31Not applicableCanada
Char-flo With Sorbitol - SusActivated charcoal (208 mg) + Sorbitol (400 mg)SuspensionOralBallard Medical Products1997-08-202004-08-04Canada
Flat-eezeActivated charcoal (250 mg) + Simethicone (80 mg)TabletOralSeaford Pharmaceuticals Inc1998-03-202003-09-08Canada
Miracle Sos BlackActivated charcoal (0.7 g/100g) + Moringa oleifera leaf (33.8 g/100g)SoapTopicalDdoruroo Co., Ltd.2017-05-01Not applicableUs
Trousse Antipoison Pour Enfants LiqActivated charcoal (120 ml) + Ipecac (30 ml)LiquidOralProdemdis Enr.1988-12-312010-07-15Canada
Unapproved/Other Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing End
ActidoseActivated charcoal (208 mg/1mL)SuspensionOralPaddock Laboratories, LLC1983-10-01Not applicableUs
Actidose AquaActivated charcoal (208 mg/1mL)SuspensionOralPaddock Laboratories, LLC1984-01-01Not applicableUs
Activated CharcoalActivated charcoal (208 mg/1mL)SuspensionOralHF Acquisition Co LLC, DBA HealthFirst2018-12-22Not applicableUs
Charcoal ActivatedActivated charcoal (1000 mg/1g)PowderOralWoodward Pharma Services Llc2018-06-01Not applicableUs
Humco Charcoal ActivatedActivated charcoal (1000 mg/1g)PowderOralHumco Holding Group. Inc.2008-01-01Not applicableUs
Miracle Sos BlackActivated charcoal (0.7 g/100g) + Moringa oleifera leaf (33.8 g/100g)SoapTopicalDdoruroo Co., Ltd.2017-05-01Not applicableUs
W Lab Sebum Out Peel Off PackActivated charcoal (2 g/100mL)GelTopicalWow Ventures2016-08-012017-08-28Us
CAS number
Average: 12.011
Monoisotopic: 12.0
Chemical Formula
InChI Key



Used as a antidote to treat poisonings following excessive oral ingestion of certain medications or poisons.


Activated charcoal is used as a gastric decontamination agent in emergency clinical settings in case of poison or medication overdose. Studies show that early administration of one dose of activated charcoal can adsorb poison in the stomach and reduce absorption while it also works long after ingestion, by interruption of enterohepatic and enterovascular cycling of poison.

Mechanism of action

Active charcoal acts by binding to the pharmaceutical drugs or poisons such as organophosphates and decreasing the systemic absorption of toxic agents. Molecules with large volume of distribution, thus likely having higher lipid solubility, tends to bind have better absorptive binding to activated charcoal. Following the administration of activated charcoal, cathartics are indicated to evacuate the charcoal-poison bonded complex from the gastrointestinal tract. Activated charcoal may also have an effect on systemic drug levels by lowering the serum levels of already absorbed drugs or toxins. Many absorbed drugs that undergo significant hepatic metabolism and conjugation are eliminated via bile into the small intestines. When they reach the small intestines, drug conjugates can undergo hydrolysis and return to the enterohepatic circulation. Activated charcoal interferes with this process and binds to the conjugated drug before hydrolysis or the free deconjugated drug before reabsorption.

Additional Data Available
Adverse Effects

Comprehensive structured data on known drug adverse effects with statistical prevalence. MedDRA and ICD10 ids are provided for adverse effect conditions and symptoms.

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Additional Data Available

Structured data covering drug contraindications. Each contraindication describes a scenario in which the drug is not to be used. Includes restrictions on co-administration, contraindicated populations, and more.

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Additional Data Available
Blackbox Warnings

Structured data representing warnings from the black box section of drug labels. These warnings cover important and dangerous risks, contraindications, or adverse effects.

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No evidence of systemic absorption of activated charcoal

Volume of distribution
Not Available
Protein binding
Not Available
Not Available
Route of elimination

Fecal excretion.

Half life
Not Available
Not Available

Adverse effects from the treatment include aspiration into the lungs and possibly pneumonitis, black stools, vomiting, and constipation or diarrhea. The oral LD50 value in rats is 15400mg/kg.

Affected organisms
  • Humans and other mammals
Not Available
Pharmacogenomic Effects/ADRs
Not Available


Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
AcetyldigoxinActivated charcoal may increase the excretion rate of Acetyldigoxin which could result in a lower serum level and potentially a reduction in efficacy.
DigoxinActivated charcoal may increase the excretion rate of Digoxin which could result in a lower serum level and potentially a reduction in efficacy.
LeflunomideActivated charcoal can cause a decrease in the absorption of Leflunomide resulting in a reduced serum concentration and potentially a decrease in efficacy.
MetildigoxinActivated charcoal may increase the excretion rate of Metildigoxin which could result in a lower serum level and potentially a reduction in efficacy.
OlanzapineThe serum concentration of Olanzapine can be decreased when it is combined with Activated charcoal.
TeriflunomideActivated charcoal can cause a decrease in the absorption of Teriflunomide resulting in a reduced serum concentration and potentially a decrease in efficacy.
Additional Data Available
  • Extended Description
    Extended Description

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  • Severity

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  • Evidence Level
    Evidence Level

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  • Action

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Food Interactions
  • Take with or without food. Give a higher dose of activated charcoal if it is administered after a large meal.


General References
  1. Shimoishi K, Anraku M, Kitamura K, Tasaki Y, Taguchi K, Hashimoto M, Fukunaga E, Maruyama T, Otagiri M: An oral adsorbent, AST-120 protects against the progression of oxidative stress by reducing the accumulation of indoxyl sulfate in the systemic circulation in renal failure. Pharm Res. 2007 Jul;24(7):1283-9. Epub 2007 Mar 27. [PubMed:17387602]
  2. Eddleston M, Juszczak E, Buckley NA, Senarathna L, Mohamed F, Dissanayake W, Hittarage A, Azher S, Jeganathan K, Jayamanne S, Sheriff MR, Warrell DA: Multiple-dose activated charcoal in acute self-poisoning: a randomised controlled trial. Lancet. 2008 Feb 16;371(9612):579-87. doi: 10.1016/S0140-6736(08)60270-6. [PubMed:18280328]
  3. Zawahir S, Gawarammana I, Dargan PI, Abdulghni M, Dawson AH: Activated charcoal significantly reduces the amount of colchicine released from Gloriosa superba in simulated gastric and intestinal media. Clin Toxicol (Phila). 2017 May 23:1-5. doi: 10.1080/15563650.2017.1325897. [PubMed:28535126]
  4. Ronowicz J, Kupcewicz B, Palkowski L, Krysinski J: Development and optimization of the activated charcoal suspension composition based on a mixture design approach. Acta Pharm. 2015 Mar;65(1):83-90. doi: 10.1515/acph-2015-0005. [PubMed:25781707]
  5. Moon J, Chun B, Song K: An exploratory study; the therapeutic effects of premixed activated charcoal-sorbitol administration in patients poisoned with organophosphate pesticide. Clin Toxicol (Phila). 2015 Feb;53(2):119-26. doi: 10.3109/15563650.2014.1001516. Epub 2015 Jan 22. [PubMed:25608917]
  6. Yousefi G, Bizhani M, Jamshidzadeh A, Gholamzadeh S: Comparison of activated charcoal and sodium polystyrene sulfonate resin efficiency on reduction of amitriptyline oral absorption in rat as treatments for overdose and toxicities. Iran J Basic Med Sci. 2017 Jan;20(1):46-52. doi: 10.22038/ijbms.2017.8092. [PubMed:28133524]
  7. Derlet RW, Albertson TE: Activated charcoal--past, present and future. West J Med. 1986 Oct;145(4):493-6. [PubMed:3538661]
  8. Spector R, Park GD: New roles for activated charcoal. West J Med. 1986 Oct;145(4):511-2. [PubMed:3788134]
  9. Guss DA: Emergency medicine: activated charcoal-the first-line agent in cases of overdose. West J Med. 1989 Jul;151(1):63. [PubMed:18750603]
  10. Neuvonen PJ: Clinical pharmacokinetics of oral activated charcoal in acute intoxications. Clin Pharmacokinet. 1982 Nov-Dec;7(6):465-89. [PubMed:6761032]
  11. World Health Organization Model List of Essential Medicines (19th List) [Link]
  12. World Health Organization Model Formulary2008 [Link]
External Links
PubChem Compound
PubChem Substance
ATC Codes
A07BA51 — Medicinal charcoal, combinationsA07BA01 — Medicinal charcoal
AHFS Codes
  • 56:04.00 — Antacids and Adsorbents
  • 56:10.00 — Antiflatulents
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Clinical Trials

Clinical Trials
0RecruitingSupportive CareHealthy Adult Volunteers1
1CompletedNot AvailableHealthy Volunteers1
1CompletedTreatmentChronic Obstructive Pulmonary Disease (COPD)1
1CompletedTreatmentMajor Depressive Disorder (MDD)1
2CompletedTreatmentHepatic Encephalopathy (HE)1
2CompletedTreatmentIrritable Bowel Syndrome (IBS)1
2CompletedTreatmentMild Hepatic Encephalopathy1
2CompletedTreatmentPlasmodium Infections / Severe Malaria1
2Not Yet RecruitingTreatmentChronic Kidney Disease stage31
2TerminatedTreatmentGastro-esophageal Reflux Disease (GERD)1
3CompletedTreatmentChronic Kidney Disease (CKD)2
3CompletedTreatmentFecal Incontinence1
3CompletedTreatmentInflammatory Bowel Diseases (IBD) / Intestinal Fistula1
4CompletedTreatmentAST-120 / Chronic Kidney Disease (CKD)1
4CompletedTreatmentChronic Kidney Disease (CKD)1
4CompletedTreatmentLoss of Solute Clearance1
4Not Yet RecruitingTreatmentAnticoagulants; Circulating, Hemorrhagic Disorder1
4Unknown StatusTreatmentChronic Renal Failure (CRF)1
Not AvailableCompletedTreatmentPhenytoin Toxicity1


Not Available
Not Available
Dosage forms
SuspensionOral208 mg/1mL
CapsuleOral225 mg
Powder, for solutionOral
PowderOral1000 mg/1g
PelletOral25 g/25g
SuspensionOral50 g/240mL
GelTopical2 g/100mL
Not Available
Not Available


Experimental Properties
water solubilityInsolubleMSDS
Predicted Properties
Water Solubility0.0 mg/mLALOGPS
Physiological Charge0ChemAxon
Hydrogen Acceptor Count0ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area0 Å2ChemAxon
Rotatable Bond Count0ChemAxon
Refractivity13.11 m3·mol-1ChemAxon
Polarizability1.51 Å3ChemAxon
Number of Rings0ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted ADMET features
Not Available


Mass Spec (NIST)
Not Available
SpectrumSpectrum TypeSplash Key
Predicted GC-MS Spectrum - GC-MSPredicted GC-MSNot Available
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSNot Available


This compound belongs to the class of organic compounds known as organic compounds. These are compounds that contain at least one carbon atom, excluding isocyanide/cyanide and their non-hydrocarbyl derivatives, thiophosgene, carbon diselenide, carbon monosulfide, carbon disulfide, carbon subsulfide, carbon monoxide, carbon trioxide, carbon suboxide, and dicarbon monoxide.
Organic compounds
Super Class
Not Available
Not Available
Sub Class
Not Available
Direct Parent
Organic compounds
Alternative Parents
Not Available
Organic compound / Aliphatic acyclic compound
Molecular Framework
Aliphatic acyclic compounds
External Descriptors
nonmetal atom, carbon group element atom (CHEBI:27594)

Drug created on October 29, 2015 08:53 / Updated on July 09, 2020 11:59

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