PREFOL-DHA- folic acid, ascorbic acid, calcium, iron, cholecalciferol, .alpha.-tocopherol, d-, pyridoxine hydrochloride, doconexent and docusate sodium capsule, liquid filled 
Method Pharmaceuticals, LLC

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.

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PreFol-DHA™
Capsules

Rx Only

DESCRIPTION:

PreFol-DHA™ is a prescription prenatal/postnatal multivitamin/mineral softgel capsule with fish oil-based DHA. PreFol-DHA™ are oblong, maroon softgel capsules with “M100” imprinted on one side.

Each capsule has the following active ingredient:
Folic Acid................................................................................1.2 mg

Each capsule also contains the following ingredients for nutritional supplementation:
Vitamin C
(ascorbic acid) ...................................................... 28 mg
Calcium (tribasic calcium phosphate) ................................. 160 mg
Iron (ferrous fumarate) ......................................................... 26 mg
Vitamin D3 (cholecalciferol) ................................................. 400 IU
Vitamin E (d-alpha tocopherol).............................................. 30 IU
Vitamin B6 (pyridoxine hydrochloride) ................................ 25 mg
DHA (Docosahexaenoic Acid)............................................... 300 mg*
Docusate Sodium................................................................ 55 mg
*from approximately 350 mg of Omega-3s derived from approximately 380 mg

Inactive Ingredients:

Capsules (Gelatin, Glycerin, Purified Water, FD&C Red #40, Titanium Dioxide, Ethyl Vanillin, FD&C Yellow #6, FD&C Blue #1), Lecithin, Soybean Oil, Yellow Bees Wax, Citric Acid, Natural Creamy Orange Flavor.

INDICATIONS AND USAGE:

PreFol-DHA™ is indicated for the supplemental requirements of patients with nutritional deficiencies or are in need of nutritional supplementation.

CONTRAINDICATIONS:

PreFol-DHA™ is contraindicated in patients with a known hypersensitivity to any of the ingredients, including fish or fish oil. Do not take this product if you are presently taking mineral oil, unless directed by a doctor.

WARNINGS:

Daily ingestion of more than 3 grams per day of omega-3 fatty acids (ALA, EPA, and DHA) from fish oils may have potential antithrombotic activities, or effects, and may increase bleeding times. Administration of omega-3 fatty acids - including DHA, should be avoided in patients with inherited or acquired bleeding diatheses, including those taking anticoagulants.

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

THIS PRODUCT CONTAINS SOYBEAN OIL AND FISH OIL.

CAUTION:

Exercise caution to ensure that the prescribed dosage of DHA does not exceed 1 gram (1000 mg) per day.

PRECAUTIONS: General:

Folates (including folic acid and reduced folates), when administered as a single agent in doses above 0.1 mg daily, may obscure the detection of B12 deficiency (specifically, the administration of folic acid may reverse the hematological manifestations of B12 deficiency, including pernicious anemia, while not addressing the neurological manifestations). Reduced folates may be less likely than folic acid to mask vitamin B12 deficiency. Folate therapy alone is inadequate for the treatment of B12 deficiency.

PATIENT INFORMATION:

PreFol-DHA™ is a prescription vitamin for use only under the direction and supervision of a licensed physician.

INTERACTIONS:

Pyridoxine hydrochloride should not be given to patients receiving the drug levodopa, because the action of levodopa is antagonized by pyridoxine hydrochloride. However, pyridoxine hydrochloride may be used concurrently in patients receiving a preparation containing both carbidopa and levodopa. Drugs which may interact with folate include:

  • Antiepileptic drugs (AED): The AED class including, but not limited to, phenytoin, carbamazepine, primidone, valproic acid, phenobarbital and lamotrigine have been shown to impair folate absorption and increase the metabolism of circulating folate. Additionally, concurrent use of folic acid has been associated with enhanced phenytoin metabolism, lowering the levels of this AED in the blood and allowing breakthrough seizures to occur.
  • Capecitabine: Folinic acid (5-formyltetrahydrofolate) may increase the toxicity of Capecitabine.
  • Cholestyramine: Reduces folic acid absorption and reduces serum folate levels.
  • Colestipol: Reduces folic acid absorption and reduces serum folate levels.
  • Cycloserine: Reduces folic acid absorption and reduces serum folate levels.
  • Dihydrofolate Reductase Inhibitors (DHFRI): DHFRIs block the conversion of folic acid to its active forms, and lower plasma and red blood cell folate levels. DHFRIs include aminopterin, methotrexate, pyrimethamine, triamterene, and trimethoprim.
  • Fluoxetine: Fluoxetine exerts a noncompetitive inhibition of the 5-methyltetrahydrofolate active transport in the intestine.
  • Isotretinoin: Reduced folate levels have occurred in some patients taking isotretinoin.

  • Nonsteroidal Anti-inflammatory Drugs (NSAIDs): NSAIDs have been shown to inhibit some folate dependent enzymes in laboratory experiments. NSAIDs include ibuprofen, naproxen, indomethacin and sulindac.

  • Oral Contraceptives: Serum folate levels may be depressed by oral contraceptive therapy.

  • Methylprednisolone: Reduced serum folate levels have been noted after treatment with methylprednisolone.

  • Pancreatic Enzymes: Reduced folate levels have occurred in some patients taking pancreatic extracts.

  • Pentamidine: Reduced folate levels have been seen with prolonged intravenous pentamidine.

  • Smoking and alcohol: Reduced serum folate levels have been noted.

  • Sulfasalazine: Inhibits the absorption and metabolism of folic acid.

  • Metformin treatment in patients with type 2 diabetes decreases serum folate.

  • Warfarin can produce significant impairment in folate status after a 6 - month therapy.

ADVERSE REACTIONS:

Allergic sensitization has been reported following both oral and parenteral administration of folic acid, as well as possibly the use of other forms of folates, including reduced folates. Paresthesia, somnolence, nausea and headaches have been reported with pyridoxine hydrochloride.

DOSAGE AND ADMINISTRATION:

Before, during, and or after pregnancy, one tablet daily or as prescribed by a physician.

HOW SUPPLIED:

PreFol-DHA™ is dispensed in bottles of 30 softgel capsules.
PRODUCT CODE 58657-100-30
KEEP OUT OF REACH OF CHILDREN.
Rx Only

All prescriptions using this product shall be pursuant to state statutes as applicable. This is not an Orange Book product. There are no implied or explicit claims on therapeutic equivalence.

Manufactured for:
Method Pharmaceuticals, LLC
www.methodpharm.com
Rev. 08/13

RECOMMENDED USE:

Before, during and/or after pregnancy, one softgel capsule daily or as prescribed by a physician.

STORAGE:

Store at 20°-25°C (68°-77°F), excursions permitted to 15°-30°C (59°-86°F) [See USP controlled room temperature].

WARNING: Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. KEEP THIS PRODUCT OUT OF 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 (877) 250-3427.
KEEP OUT OF THE REACH OF CHILDREN.

Manufactured for:
Method Pharmaceuticals, LLC, Arlington, TX 76006
www.methodpharm.com

PRINCIPAL DISPLAY PANEL

58657-100-30
PreFol-DHA
TM
CAPSULES
Rx ONLY
30 CAPSULES

PRINCIPAL DISPLAY PANEL 58657-100-30 PreFol-DHATM CAPSULES Rx ONLY 30 CAPSULES
PREFOL-DHA 
folic acid, ascorbic acid, calcium, iron, cholecalciferol, .alpha.-tocopherol, d-, pyridoxine hydrochloride, doconexent, docusate sodium capsule, liquid filled
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:58657-100
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID1.2 mg
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID28 mg
CALCIUM (UNII: SY7Q814VUP) (CALCIUM - UNII:SY7Q814VUP) CALCIUM160 mg
IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON26 mg
CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL400 [iU]
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9) (.ALPHA.-TOCOPHEROL, D- - UNII:N9PR3490H9) .ALPHA.-TOCOPHEROL, D-30 [iU]
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z) PYRIDOXINE HYDROCHLORIDE25 mg
DOCONEXENT (UNII: ZAD9OKH9JC) (DOCONEXENT - UNII:ZAD9OKH9JC) DOCONEXENT300 mg
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM55 mg
Inactive Ingredients
Ingredient NameStrength
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
ETHYL VANILLIN (UNII: YC9ST449YJ)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
SOYBEAN OIL (UNII: 241ATL177A)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Product Characteristics
ColorBROWN (Amber) Scoreno score
ShapeCAPSULESize25mm
FlavorORANGE (Natural Creamy Orange Flavor) Imprint Code M100
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58657-100-3030 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER10/01/201312/31/2014
Labeler - Method Pharmaceuticals, LLC (060216698)

Revised: 7/2015
 
Method Pharmaceuticals, LLC