NDC 43742-1675 – Dizzy

Sus Scrofa Cerebrum 6 [hp_X]/mL; Bryonia Alba Root 8 [hp_X]/mL; Kerosene 8 [hp_X]/mL; Tobacco Leaf 8 [hp_X]/mL; Ambergris 9 [hp_X]/mL; Cyclamen Purpurascens… · Liquid · Oral

Human Otc Drug

Product NDC43742-1675

Product details

Brand name
Dizzy
Generic name
Cerebellum (Suis), Bryonia (Alba), Petroleum, Tabacum, Ambra Grisea, Cyclamen Europaeum, Natrum Salicylicum, Argentum Nitricum, Asarum Canadense, Calcarea Sulphurica, Carboneum Sulphuratum, Chininum Sulphuricum, Cocculus Indicus, Conium Maculatum, Digitalis Purpurea, Gelsemium Sempervirens, Phosphorus, Piper Methysticum, Silicea, Theridion
Labeler
Deseret Biologicals, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 22, 2020
Listing expires
December 31, 2026
Pharmacologic class
Antimalarial; Blood Coagulation Factor; Non-Standardized Plant Allergenic Extract; Phosphate Binder

Active ingredients

Uses, dosage, side effects and warnings for Dizzy →

Package NDC codes (1)

Package NDCDescriptionSince
43742-1675-130 mL in 1 BOTTLE, DROPPER (43742-1675-1)Sep 22, 2020