Ornithogalum umbellatum

ORNITHOGALUM UMBELLATUM ORAL HUMAN OTC DRUG

Ornithogalum umbellatum is an FDA drug label for the active ingredient ORNITHOGALUM UMBELLATUM 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
ORNITHOGALUM UMBELLATUM
Manufacturer
Boiron
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
0220-3820
Application
N/A
Label effective
20231114

Active ingredients

Ornithogalum umbellatum 30C (**contains 0.443 mg of the active ingredient per pellet)

Indications & Usage

Heartburn with pain while swallowing*

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.

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