Advanced Arnica Plus

Product NDC

57955-3004

11-digit product format

579553004

Labeler code

57955

Product ID

57955-3004_b5b97d8c-d4bf-4954-8b63-e06306ae64e7

Type

HUMAN OTC DRUG

Nonproprietary name

Arnica montana, Arnica montana, radix, Bellis perennis, Bryonia, Hypericum perforatum, Lithium carbonicum, Magnesia phasphorica, Phytolacca decandra, Rhus toxicdendron, Ruta gravedens

Dosage form

LIQUID

Route

ORAL

Labeler

King Bio Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2022-01-27

Marketing end

0000-00-00

Substance

ARNICA MONTANA ROOT; ARNICA MONTANA WHOLE; BELLIS PERENNIS WHOLE; BRYONIA ALBA ROOT; HYPERICUM PERFORATUM WHOLE; LITHIUM CARBONATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PHYTOLACCA AMERICANA ROOT; RUTA GRAVEOLENS FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF

Active strength

10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL

Pharmacologic classes

Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Mood Stabilizer [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

NDC exclude flag

No

Listing certified through

2023-12-31

Current FDA listing

Historical FDA.report record