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Strovite One

Generic Name: iron free multivitamin and mineral supplement
Dosage Form: tablet

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

STROVITE® ONE
Iron Free Multivitamin and Mineral Supplement

Rx

COMPOSITION

Each caplet contains:
Vitamin C (as ascorbic acid) 300 mg
Vitamin D3 (as cholecalciferol) 1000 IU
Vitamin E (as d-alpha tocopheryl succinate) 100 IU
Vitamin B1 (as thiamine HCl) 20 mg
Vitamin B2 (as riboflavin) 5 mg
Niacinamide (Vitamin B3) 25 mg
Vitamin B6 (as pyridoxine HCl) 25 mg
Folic acid 1 mg
Vitamin B12 (as cyanocobalamin) 50 mcg
Biotin 100 mcg
Pantothenic Acid (as ca pantothenate) 15 mg
Magnesium (as magnesium oxide) 50 mg
Zinc (as zinc oxide) 25 mg
Selenium (as sodium selenate) 100 mcg
Copper (as cupric sulfate) 1.5 mg
Manganese (as manganese sulfate) 1.5 mg
Chromium (as chromic chloride) 50 mcg
Carotenoids (alpha-carotene, beta-carotene, cryptoxanthin, lutein, zeaxanthin) 3000 IU
Alpha Lipoic Acid 15 mg
Lutein 5 mg

Other Ingredients: Dibasic calcium phosphate, microcrystalline cellulose, carbohydrate, croscarmellose sodium, stearic acid, gelatin, polyvinyl alcohol, silicon dioxide, titanium dioxide (as color), polyethylene glycol, sucrose, magnesium stearate, modified food starch, soybean oil, talc, ethylcellulose, ascorbyl palmitate, mixed tocophererols, sodium ascorbate, medium chain triglycerides, dl-alpha-tocopherol.
Contains: Soy

Indications and Usage for Strovite One

STROVITE® ONE is indicated to provide nutritional supplementation to support optimum vitamin and mineral levels.

Contraindications

STROVITE® ONE is contraindicated in patients with hypersensitivity to any of its components. Folic Acid is contraindicated in patients with untreated and uncomplicated pernicious anemia, and in those with anaphylactic sensitivity to folic acid.

Cyanocobalamin is contraindicated in patients with sensitivity to cobalt or to cyanocobalamin (Vitamin B12).

WARNING/PRECAUTIONS

Vitamin D supplementation should be used with caution in those with hypercalcemia or conditions that may lead to hypercalcemia such as hyperparathyroidism and those who form calcium-containing kidney stones. High doses of vitamin D can lead to elevated levels of calcium that reside in the blood and soft tissues. Bone pain, high blood pressure, formation of kidney stones, renal failure, and increased risk of heart disease can occur.

Folic acid, especially in doses above 0.1 mg daily, may obscure pernicious anemia, in that hematologic remission may occur while neurological manifestations remain progressive.

The use of folic acid doses above 1 mg daily may precipitate or exacerbate the neurological damage of vitamin B12 deficiency.

Avoid Over dosage. Keep out of the reach of children.

Drug Interactions

High doses of folic acid may result in decreased serum levels of anticonvulsant drugs.

Vitamin D supplementation should not be given with large amounts of calcium in those with hypercalcemia or conditions that may lead to hypercalcemia such as hyperparathyroidism and those who form calciumcontaining kidney stones.

Zinc can inhibit the absorption of certain antibiotics; take at least 2 hours apart to minimize interactions.

Consult appropriate references for additional specific vitamin-drug interactions.

Information for Patients

Patients should be counseled to disclose all medical conditions, including use of all medications, vitamins and supplements, pregnancy, and breastfeeding.

Pediatric Use

Not recommended for pediatric use.

Adverse Reactions

Adverse reactions have been reported with specific vitamins and minerals, but generally at levels substantially higher than those in STROVITE® ONE.

Strovite One Dosage and Administration

One caplet daily or as directed by a physician.

How is Strovite One Supplied

STROVITE® ONE is a white, oblong caplet, debossed EV0207; available in bottles of 90 caplets. 0642-0207-90 and as professional samples (0642-0207-03).

Store at room temperature 15°-30°C (59°-86°F). Avoid excessive heat and moisture.

Rx

Manufactured for:
EVERETT LABORATORIES, INC.
Chatham, NJ 07928 USA

1-877-324-9349

US Patent No. 6,863,904
Strovite® is a trademark of Everett Laboratories, Inc.

(Rev. 06/14)

PRINCIPAL DISPLAY PANEL - 3 Caplet Unit Dose Pack Carton

SAMPLE NOT FOR SALE
0642-0207-03

Iron Free
Strovite® ONE Caplets
Multivitamin and Mineral Supplement

ONE THOUSAND (1000 IU VITAMIN D3)
ONE CAPLET DAILY
• FOLIC ACID
• LUTEIN
• VITAMIN C
• ZINC
• SELENIUM

The
All-in-ONE
prescription
multivitamin

UNIT DOSE PACK
3 Caplets

U.S. PATENTED

RX
GLUTEN AND LACTOSE FREE

Strovite One   CAPLETS
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 tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0642-0207
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Vitamin A (Vitamin A) Vitamin A 3000 [iU]
Calcium Pantothenate (Pantothenic Acid and Calcium Cation) Pantothenic Acid 15 mg
Ascorbic Acid (Ascorbic Acid) Ascorbic Acid 300 mg
Cholecalciferol (Cholecalciferol) Cholecalciferol 1000 [iU]
.Alpha.-Tocopherol Succinate, D- (.ALPHA.-TOCOPHEROL, D-) .Alpha.-Tocopherol Succinate, D- 100 [iU]
Thiamine (Thiamine Ion) Thiamine 20 mg
Riboflavin (Riboflavin) Riboflavin 5 mg
Niacinamide (Niacinamide) Niacinamide 25 mg
Pyridoxine Hydrochloride (Pyridoxine) Pyridoxine Hydrochloride 25 mg
Folic Acid (Folic Acid) Folic Acid 1 mg
Biotin (Biotin) Biotin 100 ug
Cyanocobalamin (Cyanocobalamin) Cyanocobalamin 50 ug
Selenium (Selenium) Selenium 100 ug
Magnesium Oxide (Magnesium Cation) Magnesium Cation 50 mg
Zinc Oxide (Zinc Oxide) Zinc Oxide 25 mg
Cupric Sulfate (Cupric Cation) Cupric Cation 1.5 mg
Manganese (Manganese) Manganese 1.5 mg
Chromium (Chromium) Chromium 50 ug
.Alpha.-Lipoic Acid (.Alpha.-Lipoic Acid) .Alpha.-Lipoic Acid 15 mg
Lutein (Lutein) Lutein 5 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM  
Cellulose, Microcrystalline  
SILICON DIOXIDE  
TITANIUM DIOXIDE  
GELATIN  
MAGNESIUM STEARATE  
POLYVINYL ALCOHOL  
STARCH, CORN  
SOYBEAN OIL  
TALC  
SUCROSE  
ETHYLCELLULOSES  
POLYETHYLENE GLYCOLS  
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS  
ASCORBYL PALMITATE  
TOCOPHEROL  
SODIUM ASCORBATE  
MEDIUM-CHAIN TRIGLYCERIDES  
.ALPHA.-TOCOPHEROL, DL-  
Product Characteristics
Color WHITE Score no score
Shape OVAL Size 19mm
Flavor Imprint Code EV0207
Contains         
Packaging
# Item Code Package Description
1 NDC:0642-0207-90 90 TABLET in 1 BOTTLE
2 NDC:0642-0207-03 1 BLISTER PACK in 1 BOX
2 3 TABLET in 1 BLISTER PACK
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG OTHER 05/04/2001
Labeler - Everett Laboratories, Inc. (071170534)
Revised: 09/2014
 
Everett Laboratories, Inc.

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