NDC 43742-1600 – Bio Tonsilla Phase

Solanum Dulcamara Top 4 [hp_X]/mL; Echinacea Angustifolia Whole 4 [hp_X]/mL; Horse Chestnut 6 [hp_X]/mL; Antimony Potassium Tartrate 6 [hp_X]/mL; Ascorbic Acid… · Liquid · Oral

Human Otc Drug

Product NDC43742-1600

Product details

Brand name
Bio Tonsilla Phase
Generic name
Dulcamara, Echinacea (Angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbicum Acidum, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (Pratensis), Sarcolacticum Acidum, Acetylcholine Chloride, Mannose, Conium Maculatum, Lymph Node (Suis), Sulphur, Calcarea Phosphorica, Funiculus Umbilicalis Suis, Hepar Suis, Hypothalamus Suis, Medulla Ossis Suis, Spleen (Suis), Cortisone Aceticum, Glandula Suprarenalis Suis, Mercurius Solubilis, Thyroidinum (suis),
Labeler
Deseret Biologicals, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
October 29, 2019
Listing expires
December 31, 2026
Pharmacologic class
Blood Coagulation Factor; Cholinergic Receptor Agonist; Corticosteroid; Phosphate Binder; Vitamin C

Active ingredients

Uses, dosage, side effects and warnings for Bio Tonsilla Phase →

Package NDC codes (1)

Package NDCDescriptionSince
43742-1600-130 mL in 1 BOTTLE, DROPPER (43742-1600-1)Oct 29, 2019