NDC 55714-2562 – Hay Fever

Lilium Lancifolium Whole Flowering 15 [hp_X]/mL; Sodium Chloride 15 [hp_X]/mL; Populus Balsamifera Leaf Bud 15 [hp_X]/mL; Anemone Pulsatilla 15 [hp_X]/mL;… · Liquid · Oral

Human Otc Drug

Product NDC55714-2562

Product details

Brand name
Hay Fever
Generic name
Apis mellifica, Echinacea, Hydrastis canadensis, Taraxacum officinale, Aconitum napellus, Alfalfa, Allium cepa, Ambrosia artemisiaefolia, Ammonium carbonicum, Aralia racemosa, Arsenicum album, Artemisia vulgaris, Arundo mauritanica, Bellis perennis, Berberis vulgaris, Bryonia, Calluna vulgaris, flos, Chelidonium majus, Chenopodium anthelminticum, Cistus canadensis, Drosera, Dulcamara, Eupatorium perfoliatum, Euphrasia officinalis, Fagus sylvatica, Fraxinus americana, Gelsemium sempervirens
Labeler
Newton Laboratories, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
May 18, 2020
Listing expires
December 31, 2026
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Osmotic Laxative; Standardized Insect Venom Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Hay Fever →

Package NDC codes (1)

Package NDCDescriptionSince
55714-2562-130 mL in 1 BOTTLE, GLASS (55714-2562-1)May 18, 2020