Strovite One

Product NDC

0642-0207

11-digit product format

006420207

Labeler code

0642

Product ID

0642-0207_30c8e7e7-7cba-c12f-e063-6394a90a41e9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Vitamin A, Calcium Pantothenate, Ascorbic Acid, Cholecalciferol, .Alpha.-Tocopherol Succinate, D-, Thiamine, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Biotin, Cyanocobalamin, Selenium, Magnesium Oxide, Zinc Oxide, Cupric Sulfate, Manganese, Chromium, .Alpha.-Lipoic Acid, and Lutein

Dosage form

TABLET

Route

ORAL

Labeler

Exeltis USA, Inc.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2001-05-04

Substance

.ALPHA.-TOCOPHEROL SUCCINATE, D-; ALPHA LIPOIC ACID; ASCORBIC ACID; BIOTIN; CALCIUM PANTOTHENATE; CHOLECALCIFEROL; CHROMIUM; CUPRIC SULFATE; CYANOCOBALAMIN; FOLIC ACID; LUTEIN; MAGNESIUM OXIDE; MANGANESE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SELENIUM; THIAMINE; VITAMIN A; ZINC OXIDE

Active strength

45; 15; 300; 100; 7.5; 25; 50; 1.5; 50; 1700; 5; 50; 1.5; 25; 25; 5; 100; 20; 900; 25 ug/1; mg/1; mg/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1

Pharmacologic classes

Allergens [CS], Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], 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 D [CS], Vitamin D [EPC]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes