PTS/Stress

Product NDC

43742-1206

11-digit product format

437421206

Labeler code

43742

Product ID

43742-1206_22e3c180-7725-43b2-978f-ddb236c288fb

Type

HUMAN OTC DRUG

Nonproprietary name

Kali Phosphoricum, Ambra Grisea, Cacao, Lithium Carbonicum, Phosphoricum Acidum, Arnica Montana, Aconitum Napellus, Calcarea Carbonica, Cerebrum Suis, Glandula Suprarenalis Suis, Argemone Mexicana, Arsenicum Album, Cicuta Virosa, Hyoscyamus Niger, Ignatia Tigrinum, Natrum Muriaticum, Tarentula Hispanica, Stramonium, Buthus Australis

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2018-04-12

Marketing end

2023-05-22

Substance

DIBASIC POTASSIUM PHOSPHATE; AMBERGRIS; COCOA; LITHIUM CARBONATE; PHOSPHORIC ACID; ARNICA MONTANA; ACONITUM NAPELLUS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SUS SCROFA CEREBRUM; SUS SCROFA ADRENAL GLAND; ARGEMONE MEXICANA; ARSENIC TRIOXIDE; CICUTA VIROSA ROOT; HYOSCYAMUS NIGER; STRYCHNOS IGNATII SEED; LILIUM LANCIFOLIUM WHOLE FLOWERING; SODIUM CHLORIDE; LYCOSA TARANTULA; DATURA STRAMONIUM; ANDROCTONUS AUSTRALIS VENOM

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record