Carbo vegetabilis

ACTIVATED CHARCOAL ORAL HUMAN OTC DRUG

Carbo vegetabilis is an FDA drug label for the active ingredient ACTIVATED CHARCOAL manufactured by Boiron administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231109.

Generic name
ACTIVATED CHARCOAL
Manufacturer
Boiron
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
0220-1197
Application
N/A
Label effective
20231109

Active ingredients

Carbo vegetabilis 1M (**contains 0.443 mg of the active ingredient per pellet)

Indications & Usage

Abdominal Bloating With Gas*

Dosage & Administration

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Contraindications

Not available.

Warnings

Not available.

Adverse Reactions

Not available.