Arnicare Leg Cramps

Product NDC

0220-9079

11-digit product format

002209079

Labeler code

0220

Product ID

0220-9079_1c320dfd-afb8-9ac2-e063-6394a90a397e

Type

HUMAN OTC DRUG

Nonproprietary name

ARNICA MONTANA WHOLE, COPPER, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, STRYCHNOS NUX-VOMICA SEED, PASSIFLORA INCARNATA TOP, CLAVICEPS PURPUREA SCLEROTIUM

Dosage form

TABLET

Route

ORAL

Labeler

Laboratoires Boiron

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2023-09-11

Substance

ARNICA MONTANA; CLAVICEPS PURPUREA SCLEROTIUM; COPPER; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PASSIFLORA INCARNATA TOP; STRYCHNOS NUX-VOMICA SEED

Active strength

6; 9; 4; 6; 3; 6 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_X]/1; [hp_C]/1

Pharmacologic classes

Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes