NDC 43857-0580 – Scrofularoforce

Rumex Crispus Root 3 [hp_X]/mL; Zanthoxylum Americanum Bark 3 [hp_X]/mL; Sus Scrofa Lymph 8 [hp_X]/mL; Scrophularia Nodosa Whole 8 [hp_X]/mL; Barium Carbonate… · Liquid · Oral

Human Otc Drug

Product NDC43857-0580

Product details

Brand name
Scrofularoforce
Generic name
Rumex Crispus, Xanthoxylum Fraxineum, Lymph Node (Suis), Scrophularia Nodosa, Baryta Carbonica, Baryta Muriatica, Belladonna, Calcarea Carbonica, Conium Maculatum, Helleborus Niger, Iodium, Kali Phosphoricum, Lachesis Mutus, Natrum Phosphoricum, Silicea, Juniperus Virginiana
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
February 18, 2021
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Scrofularoforce →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0580-130 mL in 1 BOTTLE, DROPPER (43857-0580-1)Feb 18, 2021