Multi Vitamin and Fluoride

Product NDC

51862-162

11-digit product format

518620162

Labeler code

51862

Product ID

51862-162_4b167374-e94b-46d7-b439-802b7782250a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Multivitamin and Fluoride

Dosage form

SOLUTION/ DROPS

Route

ORAL

Labeler

Mayne Pharma Inc

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2011-05-21

Marketing end

2019-10-31

Substance

VITAMIN A PALMITATE; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL; THIAMINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN; SODIUM FLUORIDE

Active strength

1500 [iU]/mL; mg/mL; [iU]/mL; [iU]/mL; mg/mL; mg/mL; mg/mL; mg/mL; ug/mL; mg/mL

Pharmacologic classes

Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record