AMBROSIA ARTEMISIAEFOLIA
AMBROSIA ARTEMISIAEFOLIA is an FDA drug label for the active ingredient AMBROSIA ARTEMISIIFOLIA 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 20231208.
Generic: AMBROSIA ARTEMISIIFOLIA
Manufacturer: Boiron
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 0220-0230
Application:
Effective: 20231208
Active Ingredients: Ambrosia artemisiaefolia 200CK Active ingredient**: See product name on front panel (**contains 0.443 mg of the active ingredient per pellet).
Indications & Usage
Relieves symptoms of hay fever * See symptoms on front panel.
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.
More from same ingredient
No related products.