Bio Co-Enzyme Phase

Product NDC

43742-0896

Requested package NDC

43742-0896-1

11-digit product format

437420896

Labeler code

43742

Product ID

43742-0896_8b66f865-133c-4f3b-8bdc-5ab6ade6b8d9

Type

HUMAN OTC DRUG

Nonproprietary name

Beta Vulgaris, Ascorbic Acid, Cysteinum, Natrum Oxalaceticum, Nicotinamidum, Pulsatilla (Vulgaris), Pyridoxinum, Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Adrenalinum, Aconiticum Acidum, Cis, Alpha-Ketoglutaricum Acidum, Alpha-Lipoicum Acidum, Cerium Oxalicum, Citricum Acidum, Fumaricum Acidum, Magnesium Oroticum Dihydricum, Malicum Acidum, Nadidum, Natrum Pyruvicum, Pantothenic Acid, Succinicum Acidum, Adenosinum Triphosphoricum Dinatrum, Hepar Sulphuris Calcareum, Sulphur

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2017-02-22

Marketing end

2021-11-22

Substance

BETA VULGARIS; ASCORBIC ACID; CYSTEINE; SODIUM DIETHYL OXALACETATE; NIACINAMIDE; PULSATILLA VULGARIS; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; EPINEPHRINE; ACONITIC ACID, (Z)-; OXOGLURIC ACID; THIOCTIC ACID; CEROUS OXALATE NONAHYDRATE; ANHYDROUS CITRIC ACID; FUMARIC ACID; MAGNESIUM OROTATE DIHYDRATE; MALIC ACID; NADIDE; SODIUM PYRUVATE; PANTOTHENIC ACID; SUCCINIC ACID; ADENOSINE TRIPHOSPHATE DISODIUM; CALCIUM SULFIDE; SULFUR; MANGANESE PHOSPHATE, DIBASIC; BARIUM OXALOSUCCINATE; PROTEUS MORGANII

Active strength

4 [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_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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record