Drugs Details

Drugs Info of Zenate Prenatal
Drugs Details
  • Drugs Type  : FDA
  • Date : 14th Jul 2015 08:08 am
  • Brand Name : Zenate Prenatal
  • Generic Name : (Vitamins Prenatal with Zinc)

Prenatal Multivitamin/ Mineral Supplement Tablets


Accidental overdose of iron-containing products is a leading cause of fetal poisoning in children under six. Keep this product out of the reach of children. In case of accidental overdose, call a doctor or poison control center immediately.


Each film-coated tablet contains:

3000 I.U.
D (as cholecalciferol)
400 I.U.
E (as dl-alpha tocopheryl acetate)
10 I.U.
C (ascorbic acid)
70 mg
Folic Acid
1 mg
B1 (as thiamine mononitrate)
1.5 mg
B2 (riboflavin)
1.6 mg
B6 (as pyridoxine hydrochloride)
2.2 mg
B12 (cyanocobalamin)
2.2 µg
Niacin (as niacinamide)
Calcium (from calcium carbonate)
200 mg
Iodine (from potassium iodide)
175 µg
Iron (from ferrous fumarate)
65 mg
Magnesium (from magnesium oxide)
100 mg
Zinc (from zinc oxide)
15 mg
          * Input as retinyl


        and beta-carotene

Inactive Ingredients:
Amorphous Precipitated Silica, Aqueous Shellac, Croscarmellose Sodium, Crospovidone, Hydrogenated Soybean Oil, Hydrogenated Castor Oil, Hydroxypropyl Cellulose, Hydroxylpropyl Methylcellulose, Magnesium Stearate, Polyethylene Glycol, Polysorbate 80, Powdered Cellulose, Pregelatinized Starch and Titanium Dioxide.


As a dietary adjunct in nutritional stress associated with periconception, pregnancy and lactation.

Dosage Administration

One tablet daily or as directed by physician.

How Supplied

Advanced Formula ZENATE® Tablets are white, film-coated scored, capsule-shaped tablets debossed "SOLVAY" on one side and "1472" on the other and supplied in child-resistant unit dose foil pouches.

Unit dose pack of 30 tablets (1 x 30) NDC 0032-1472-26.

Advanced Formula ZENATE® Tablets are supplied in child-resistant unit dose packaging. Do not repackage.

Store at controlled room temperature: 15°- 30° C (59°- 86° F)

CAUTION: Federal Law prohibits dispensing without prescription.

Side Effects

Allergic sensitization has been reported following both oral and parenteral adiministration of folic acid.


No information provided.




Folic acid may obscure pernicious anemia, in that hematologic remission can occur while neurologic manifestations remain progressive.


No information provided.


This product is contraindicated in patients with a known hypersensitivity to any of the ingredients.

Clinical Pharamacology

No information provided.

Patient Information

Do not remove tablets from original unit-dose, child-resistant packaging until use.

Consumer Overview Uses

No Information Available!

Consumer Overview Side Effect

No Information Available!

Consumer Overview Missed Dose

No Information Available!

Patient Detailed Side Effect

No Information Available!

Patient Detailed How Take

No Information Available!

Patient Detailed Avoid Taking

No Information Available!

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