NDC 70163-0031 – Pollen Hayfever

Epinephrine 6 [hp_X]/mL; Onion 6 [hp_X]/mL; Ambrosia Artemisiifolia Whole 12 [hp_X]/mL; Arsenic Triiodide 6 [hp_X]/mL; Artemisia Vulgaris Pollen 12 [hp_X]/mL;… · Liquid · Oral

Human Otc Drug

Product NDC70163-0031

Product details

Brand name
Pollen Hayfever
Generic name
Adrenalinum, Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Iodatum, Mugwort Pollen (Artemisia Vulgaris), Bellis Perennis, Brassica SPP, Chenopodium Album, Euphrasia Officinalis, Histaminum Hydrochloricum, Alfalfa Pollen (Medicago Sativa), Phleum Pratense, Yellow Dock Pollen (Rumex Crispus), Sabadilla, Silicea, Goldenrod Pollen (Solidago Canadensis), Dandelion Pollen (Taraxacum Officinale), Red Clover Pollen (Trifolium Pratense), Xanthium Strumarium
Labeler
NaturalCare
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
May 5, 2026
Listing expires
December 31, 2027
Pharmacologic class
Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Pollen Allergenic Extract; Non-Standardized Pollen Allergenic Extract; Non-Standardized Pollen Allergenic Extract; Non-Standardized Pollen Allergenic Extract; Non-Standardized Pollen Allergenic Extract; Non-Standardized Pollen Allergenic Extract; Non-Standardized Pollen Allergenic Extract; Non-Standardized Pollen Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Pollen Hayfever →

Package NDC codes (1)

Package NDCDescriptionSince
70163-0031-21 BOTTLE, DROPPER in 1 CARTON (70163-0031-2) / 30 mL in 1 BOTTLE, DROPPER (70163-0031-1)May 5, 2026