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NataFort Package Insert

Status:
Prescription (Rx) Boxed warning Facts
Strength:
120 mg, 400 IU, 11 IU, 2 mg, 3 mg, 20 mg, 10 mg, 1 mg, 12 mcg, 60 mg
Drug class:
Active ingredients:
Similar drugs:

Source: FDA drug labeling via NLM DailyMed · About this document

Prescribing information (package insert) - NataFort

DESCRIPTION

NataFort® is a prescription prenatal/postnatal multivitamin/mineral supplement. The tablet is white, coated, and oval in shape, and is debossed "N1" on one side and is blank on the other.

Each prenatal tablet contains:
Vitamin C (Ascorbic acid)120 mg
Vitamin D3 (Cholecalciferol)400 IU
Vitamin E (dl-alpha tocoperyl acetate)11 IU
Thiamin (Vitamin B1)2 mg
Riboflavin (Vitamin B2)3 mg
Niacinamide (Vitamin B3)20 mg
Vitamin B6 (Pyridoxine HCl)10 mg
Folic Acid1 mg
Vitamin B12 (Cyanocobalamin)12 mcg
Iron (Ferrous fumarate, carbonyl iron)60 mg

INDICATIONS

NataFort® is a multivitamin/mineral prescription drug indicated for use in improving the nutritional status of women prior to conception, throughout pregnancy, and in the postnatal period for both lactating and nonlactating mothers.

CONTRAINDICATIONS

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

WARNING

Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. KEEP THIS PRODUCT OUT OF THE REACH OF CHILDREN. In case of accidental overdose, call a doctor or poison control center immediately.

WARNING

Folic acid alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where vitamin B12 is deficient.

PRECAUTIONS

Folic acid in doses above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress.

ADVERSE REACTIONS

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

DOSAGE AND ADMINISTRATION

One tablet daily or as directed by a physician.

Store at controlled room temperature.

NOTICE: Contact with moisture can discolor or erode the tablet.

HOW SUPPLIED

Bottles of 90 tablets each - NDC 0178-0716-90.

US Patent 6,521,247

MISSION PHARMACAL COMPANY

San Antonio, TX USA 78230 1355

Copyright © 2011 Mission Pharmacal Company.

All rights reserved.

L071690 C01 Rev 005110

About this document

Source: FDA drug labeling via NLM DailyMed · View the label on DailyMed

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for NataFort

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Boxed warning Yes – this drug has a boxed warning (also called a black box warning), the strongest warning of the FDA.
Drug class Vitamin B12, Vitamin B6 Analog, Vitamin C, Vitamin D
Active ingredients Ascorbic acid 120 mg, Cholecalciferol 400 IU, Alpha-tocopherol acetate, dl- 11 IU, Thiamine mononitrate 2 mg, Riboflavin 3 mg, Niacinamide 20 mg, Pyridoxine hydrochloride 10 mg, Folic acid 1 mg, Cyanocobalamin 12 mcg, Iron 60 mg
Dosage form Tablet
Route Oral
Marketing status not in the current FDA NDC Directory
Company (applicant) Mission Pharmacal Company
FDA approval UNAPPROVED DRUG OTHERUnapproved drug
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
120 mg, 400 IU, 11 IU, 2 mg, 3 mg, 20 mg, 10 mg, 1 mg, 12 mcg, 60 mg – 90 in 1 bottle NDC 0178-0716-90

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.