Breathe

Product NDC

43742-0810

11-digit product format

437420810

Labeler code

43742

Product ID

43742-0810_b965936a-ac40-4918-a294-691068783d33

Type

HUMAN OTC DRUG

Nonproprietary name

Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Natrum Muriaticum, Rhus Tox, Sulphur, Adenosinum Cyclophosphoricum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Lung (Suis), Mucosa Nasalis Suis, Pantothenic Acid, Sarcolacticum Acidum, Acetylcholine Chloride, Coumarinum, Malvin, Dysentery Bacillus, Proteus (Morgani)

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2016-07-13

Marketing end

2023-06-08

Substance

ACONITUM NAPELLUS; SILVER NITRATE; ARSENIC TRIOXIDE; SODIUM CHLORIDE; TOXICODENDRON PUBESCENS LEAF; SULFUR; ADENOSINE CYCLIC PHOSPHATE; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; SUS SCROFA LUNG; SUS SCROFA NASAL MUCOSA; PANTOTHENIC ACID; LACTIC ACID, L-; ACETYLCHOLINE CHLORIDE; COUMARIN; MALVIN; SHIGELLA DYSENTERIAE; PROTEUS MORGANII

Active strength

6 [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; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record