Flotrex

Product NDC

59088-020

11-digit product format

590880020

Labeler code

59088

Product ID

59088-020_399c637c-0e25-9b11-e063-6294a90a4c28

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Multivitamins, Sodium Fluoride 1 mg

Dosage form

TABLET, CHEWABLE

Route

ORAL

Labeler

PureTek Corporation

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2025-07-10

Substance

.ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CHOLECALCIFEROL; CYANOCOBALAMIN; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; SODIUM FLUORIDE; THIAMINE MONONITRATE; VITAMIN A

Active strength

6.75; 24; 10; 4.5; 300; 13.5; 1.05; 1.2; 36; 1; 1.05; 750 mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes