Glucoreg

Product NDC
43742-1291
11-digit product format
437421291
Labeler code
43742
Product ID
43742-1291_5939a5fb-2139-495b-a8f8-fb24282c2627
Type
HUMAN OTC DRUG
Nonproprietary name
Ascorbicum Acidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, DHEA (Dehydroepiandrosterone), Phloridzinum, Adenosinum Triphosphoricum Dinatrum, alpha-Lipoicum Acidum, Citricum Acidum, Fumaricum Acidum, Glyoxal Trimer Dihydrate, Nadidum, Pantothenic Acid, Acetaldehyde, Insulinum (Suis), Hepar Suis, Pancreas Suis, Glucagon, Baryta Oxalica, Alloxanum, Berberis Vulgaris, Carcinosin, Lycopodium Clavatum, Momordica Balsamina, Phosphoricum Acidum, Phosphorus
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-11-01
Marketing end
2024-04-04
Substance
ACETALDEHYDE; ADENOSINE TRIPHOSPHATE DISODIUM; ALLOXAN; ASCORBIC ACID; BARIUM OXALATE; BERBERIS VULGARIS ROOT BARK; CITRIC ACID MONOHYDRATE; FUMARIC ACID; GLUCAGON; GLYOXAL TRIMER DIHYDRATE; GYMNEMA SYLVESTRE LEAF; HUMAN BREAST TUMOR CELL; INSULIN PORK; LACTIC ACID, L-; LYCOPODIUM CLAVATUM SPORE; MOMORDICA BALSAMINA IMMATURE FRUIT; NADIDE; PANTOTHENIC ACID; PHLORIZIN; PHOSPHORIC ACID; PHOSPHORUS; PORK LIVER; PRASTERONE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SUS SCROFA PANCREAS; SYZYGIUM CUMINI SEED; THIAMINE HYDROCHLORIDE; THIOCTIC ACID; TRIGONELLA FOENUM-GRAECUM WHOLE
Active strength
8 [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/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
Pharmacologic classes
Acidifying Activity [MoA], Analogs/Derivatives [Chemical/Ingredient], Anti-coagulant [EPC], Antihypoglycemic Agent [EPC], Ascorbic Acid [CS], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased GI Motility [PE], Decreased GI Smooth Muscle Tone [PE], Decreased Glycolysis [PE], Gastrointestinal Motility Inhibitor [EPC], Increased Gluconeogenesis [PE], Increased Glycogenolysis [PE], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1291-14374212910130 mL in 1 BOTTLE, DROPPER (43742-1291-1) 30 ml2018-11-012024-04-04NoNoCurrent