BACT COMBINATION

Product NDC

43742-1698

11-digit product format

437421698

Labeler code

43742

Product ID

43742-1698_31bcd741-fde7-4f83-811a-f71139927996

Type

HUMAN OTC DRUG

Nonproprietary name

Adenosinum Triphosphoricum Dinatrum, Malicum Acidum, Natrum Oxalaceticum, Oroticum Acidum, Riboflavinum, Cinnamic Acid, Petroselinum Sativum, Colibacillinum Cum Natrum Muriaticum, Echinacea (Angustifolia), Helicobacter Pylori, Mycoplasma Pneumoniae, Proteus (Mirabilis), Proteus (Vulgaris), Pseudomonas Aeruginosa, Salmonella Typhi Nosode, Enterococcus Faecalis, Streptococcus Mutans, Pneumococcinum, Streptococcus Agalactiae, Legionella Pneumophila, Listeria Monocytogenes, Dysentery Bacillus, Shigella Sonnei,

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2020-12-01

Marketing end

2028-11-01

Substance

ADENOSINE PHOSPHATE DISODIUM; CINNAMIC ACID; ECHINACEA ANGUSTIFOLIA WHOLE; ENTEROCOCCUS FAECALIS; ESCHERICHIA COLI; HELICOBACTER PYLORI; LEGIONELLA PNEUMOPHILA; LISTERIA MONOCYTOGENES; MALIC ACID; MYCOPLASMA PNEUMONIAE; OROTIC ACID MONOHYDRATE; PETROSELINUM CRISPUM WHOLE; PROTEUS MIRABILIS; PROTEUS MORGANII; PROTEUS VULGARIS; PSEUDOMONAS AERUGINOSA; RIBOFLAVIN; SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI; SHIGELLA DYSENTERIAE; SHIGELLA SONNEI; SODIUM DIETHYL OXALACETATE; STREPTOCOCCUS AGALACTIAE; STREPTOCOCCUS DYSGALACTIAE; STREPTOCOCCUS EQUINUS; STREPTOCOCCUS MUTANS; STREPTOCOCCUS PNEUMONIAE; STREPTOCOCCUS UBERIS; STREPTOCOCCUS VIRIDANS GROUP

Active strength

6; 6; 15; 13; 15; 15; 14; 14; 6; 15; 6; 6; 15; 30; 15; 15; 6; 17; 15; 15; 6; 14; 15; 32; 13; 13; 32; 38 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

NDC exclude flag

No

Current FDA listing

Yes