Candida albicans
CANDIDA ALBICANS
ORAL
HUMAN PRESCRIPTION DRUG
Candida albicans is an FDA drug label for the active ingredient CANDIDA ALBICANS 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 20231115.
- Generic name
- CANDIDA ALBICANS
- Manufacturer
- Boiron
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 0220-6413
- Application
- N/A
- Label effective
- 20231115
Active ingredients
Candida albicans 8X (**contains 0.443 mg of the active ingredient per pellet)
Indications & Usage
Rx Only*
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.