Carbo animalis
CARBO ANIMALIS
ORAL
HUMAN OTC DRUG
Carbo animalis is an FDA drug label for the active ingredient CARBO ANIMALIS 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
- CARBO ANIMALIS
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 0220-1164
- Application
- N/A
- Label effective
- 20231109
Active ingredients
Carbo animalis 200CK (**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.