SAPONARIA OFFICINALIS
SAPONARIA OFFICINALIS ROOT
ORAL
HUMAN OTC DRUG
SAPONARIA OFFICINALIS is an FDA drug label for the active ingredient SAPONARIA OFFICINALIS ROOT 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 20231114.
- Generic name
- SAPONARIA OFFICINALIS ROOT
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 0220-4560
- Application
- N/A
- Label effective
- 20231114
Active ingredients
SAPONARIA OFFICINALIS (**contains 0.443 mg of the active ingredient per pellet)
Indications & Usage
Skin Rash With Itching*
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.