4 Kids Leg Pain Relief

Product NDC

54973-3383

11-digit product format

549733383

Labeler code

54973

Product ID

54973-3383_ee17d291-2a46-3ba7-e053-2a95a90a4ffb

Type

HUMAN OTC DRUG

Nonproprietary name

Tribasic Calcium Phosphate, Arnica Montana, Oyster Shell Calcium Carbonate, Crude, Copper, Eupatorium Perfoliatum Flowering Top, Magnesium Phosphate, Dibasic Trihydrate, Phosphorus, Guaiacum Officinale Resin and Phosphoric Acid

Dosage form

TABLET

Route

ORAL

Labeler

Hyland's Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2018-11-01

Marketing end

0000-00-00

Substance

ARNICA MONTANA; COPPER; EUPATORIUM PERFOLIATUM FLOWERING TOP; GUAIACUM OFFICINALE RESIN; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORIC ACID; PHOSPHORUS; TRIBASIC CALCIUM PHOSPHATE

Active strength

30 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

Pharmacologic classes

Calculi Dissolution Agent [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [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], 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