Pain

Product NDC

50845-0029

11-digit product format

508450029

Labeler code

50845

Product ID

50845-0029_5a6cc0b5-e104-403c-9207-3adc949b68b2

Type

HUMAN OTC DRUG

Nonproprietary name

Aconitum Napellus, Arnica Montana, Arsenicum Album, Bellis Perennis, Cartilago Suis, Causticum, Chamomilla, Coffea Cruda, Euphorbium Officinarum, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Passiflora Incarnata, Pyrogenium, Ranunculus Bulbosus, Symphytum Officinale

Dosage form

SPRAY

Route

ORAL

Labeler

Liddell Laboratories, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2010-10-28

Marketing end

2021-01-19

Substance

ACONITUM NAPELLUS; ARNICA MONTANA; ARSENIC TRIOXIDE; BELLIS PERENNIS; SUS SCROFA CARTILAGE; CAUSTICUM; MATRICARIA RECUTITA; ARABICA COFFEE BEAN; EUPHORBIA RESINIFERA RESIN; PSEUDOGNAPHALIUM OBTUSIFOLIUM; HYPERICUM PERFORATUM; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PASSIFLORA INCARNATA TOP; RANCID BEEF; RANUNCULUS BULBOSUS; COMFREY ROOT

Active strength

200 [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record