Scrofularoforce

Product NDC

43857-0479

11-digit product format

438570479

Labeler code

43857

Product ID

43857-0479_545270a3-5985-4c09-befd-4c4665d58e49

Type

HUMAN OTC DRUG

Nonproprietary name

Rumex Crispus, Scrophularia Nodosa, Xanthoxylum Fraxineum, Lymph Node (Suis), Baryta Carbonica, Baryta Muriatica, Belladonna, Calcarea Carbonica, Conium Maculatum, Helleborus Niger, Iodium, Kali Phosphoricum, Lachesis Mutus, Natrum Phosphoricum, Silicea, Juniperus Virginiana

Dosage form

LIQUID

Route

ORAL

Labeler

BioActive Nutritional, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2018-05-11

Marketing end

2023-06-20

Substance

RUMEX CRISPUS ROOT; SCROPHULARIA NODOSA; ZANTHOXYLUM AMERICANUM BARK; SUS SCROFA LYMPH; BARIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; ATROPA BELLADONNA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CONIUM MACULATUM FLOWERING TOP; HELLEBORUS NIGER ROOT; IODINE; POTASSIUM PHOSPHATE, DIBASIC; LACHESIS MUTA VENOM; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SILICON DIOXIDE; JUNIPERUS VIRGINIANA TWIG

Active strength

3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record