Active FE

Name: Active FE

What are some things I need to know or do while I take Active FE?

  • Tell all of your health care providers that you take this medicine. This includes your doctors, nurses, pharmacists, and dentists.
  • This medicine may affect certain lab tests. Tell all of your health care providers and lab workers that you take Active FE.
  • Tell your doctor if you are pregnant or plan on getting pregnant. You will need to talk about the benefits and risks of using this medicine while you are pregnant.
  • Tell your doctor if you are breast-feeding. You will need to talk about any risks to your baby.
  • If you are allergic to tartrazine, talk with your doctor. Some products have tartrazine.
  • Not all products are meant for use in children. Talk with the doctor.

If OVERDOSE is suspected

If you think there has been an overdose, call your poison control center or get medical care right away. Be ready to tell or show what was taken, how much, and when it happened.

Warnings

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

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.

Call your doctor about side effects. You may report side effects by calling GM Pharmaceuticals, Inc. at 1-888-535-0305.

PRINCIPAL DISPLAY PANEL - 30 Tablet Bottle Label

58809-725-30

Active FE™
Iron Supplement

GMPharmaceuticals, Inc.

30 Tablets
Rx

Manufactured for:
GM Pharmaceuticals, Inc.
Arlington, TX 76015

Lactose, Gluten and Sugar Free

Active FE 
.beta.-carotene, ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine hydrochloride, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, cyanocobalamin, iron pentacarbonyl, magnesium oxide, zinc oxide, and cupric oxide tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:58809-725
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
.BETA.-CAROTENE (.BETA.-CAROTENE) .BETA.-CAROTENE 2100 [iU]
ASCORBIC ACID (ASCORBIC ACID) ASCORBIC ACID 160 mg
CHOLECALCIFEROL (CHOLECALCIFEROL) CHOLECALCIFEROL 400 [iU]
.ALPHA.-TOCOPHEROL ACETATE, DL- (.ALPHA.-TOCOPHEROL, DL-) .ALPHA.-TOCOPHEROL, DL- 40 [iU]
THIAMINE HYDROCHLORIDE (THIAMINE ION) THIAMINE HYDROCHLORIDE 4 mg
RIBOFLAVIN (RIBOFLAVIN) RIBOFLAVIN 4 mg
NIACINAMIDE (NIACINAMIDE) NIACINAMIDE 20 mg
PYRIDOXINE HYDROCHLORIDE (PYRIDOXINE) PYRIDOXINE HYDROCHLORIDE 20 mg
FOLIC ACID (FOLIC ACID) FOLIC ACID 1250 ug
CYANOCOBALAMIN (CYANOCOBALAMIN) CYANOCOBALAMIN 30 ug
IRON PENTACARBONYL (FERROUS CATION) FERROUS CATION 75 mg
MAGNESIUM OXIDE (MAGNESIUM CATION) MAGNESIUM OXIDE 30 mg
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE 20 mg
CUPRIC OXIDE (CUPRIC CATION) CUPRIC CATION 1 mg
Inactive Ingredients
Ingredient Name Strength
FD&C YELLOW NO. 6  
FD&C BLUE NO. 2  
FD&C RED NO. 40  
HYPROMELLOSES  
POLYVINYL ALCOHOL  
TRIACETIN  
TALC  
TITANIUM DIOXIDE  
CROSCARMELLOSE SODIUM  
MAGNESIUM STEARATE  
CELLULOSE, MICROCRYSTALLINE  
STARCH, CORN  
SILICON DIOXIDE  
STEARIC ACID  
Product Characteristics
Color RED Score no score
Shape OVAL Size 18mm
Flavor Imprint Code FE1
Contains     
Packaging
# Item Code Package Description
1 NDC:58809-725-30 1 BOTTLE in 1 CARTON
1 30 TABLET in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG OTHER 11/11/2013
Labeler - GM Pharmaceuticals, Inc. (793000860)
Revised: 08/2014   GM Pharmaceuticals, Inc.

What are some other side effects of this drug?

All drugs may cause side effects. However, many people have no side effects or only have minor side effects. Call your doctor or get medical help if any of these side effects or any other side effects bother you or do not go away:

  • Upset stomach or throwing up.
  • Loose stools (diarrhea).
  • Hard stools (constipation).

These are not all of the side effects that may occur. If you have questions about side effects, call your doctor. Call your doctor for medical advice about side effects.

You may report side effects to the FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.

Some side effects of multivitamin with minerals may not be reported. Always consult your doctor or healthcare specialist for medical advice. You may also report side effects to the FDA.

Liver Dose Adjustments

Data not available

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