Vita-Pac Capsule - Prenatal/Postnatal/Folate Health Dietary Supplement
Supplement Facts
Serving Size: 1 Capsule
Servings per Bottle: 30
Amount Per Serving:
% Daily Value
Vitamin C (as Ascorbic Acid)
125 mg
104%
Calcium (as Calcium Carbonate from Aquamin Red Algae)
200 mg
15%
Iron (as Ferrous Bisglycinate from Ferrochel Chelate)
13 mg
72%
Vitamin D3 (as Cholecaliciferol from Veg D3)
12.5 mcg
63%
Thiamine (as Thiamine HCL)
1.4 mg
117%
Vitamin B6 (as Pyridoxal-5-Phosphate)
2.5 mg
147%
Folate (as 5-Methyltetrahydrofolate as Mangafolate-C)
900 mcg
375%
Vitamin B12 (as Methylcobalamin)
100 mcg
4,166%
OTHER INGREDIENTS: Vegetable Cellulose (Capsule), Silica Dioxide
WARNING AND PRECAUTIONS
PRECAUTIONS SECTION
This product is contraindicated in patients with a known hypersensitivity to any of the ingredients.
Vita-Pac should only be used under the direction and supervision of a licensed medical practitioner.
WARNING: Children under 18, pregnant or nursing women, and individuals with known medical conditions should consult a physician before using this or any dietary supplement.
In case of accidental overdoes, call a doctor or poison control center immediately.
KEEP OUT OF REACH OF CHILDREN
STORAGE
HEALTH CLAIM SECTION
Store at 20°-25°C (68°-77°F); excursions permitted to 15°-30°C (59°-86°F).
DOSAGE & ADMINISTRATION
DOSAGE & ADMINISTRATION SECTION
Take one (1) capsule once daily preferably with meals or as directed by medical practitioner.
If you are pregnant or nursing, ask a healthcare professional.
Vita-Pac should be administered under the supervision of a licensed medical practitioner.
HOW SUPPLIED HEALTH CLAIM:
HEALTH CLAIM SECTION
Vita-Pac
Dietary Supplement
NHRIC: 82379-1200-01 *
Bottles contain 30 Capsules
Distributed in the USA by: Trell Pharma, LLC
† The most appropriate way to ensure pedigree reporting consistent with these regulatory guidelines and safety monitoring is to dispense this product by prescription. This is not an Orange Book product.
*Trell Pharma does not represent these product codes to be National Drug Codes (NDC). Product codes are formatted according to standard industry practice, to meet the formatting requirement by pedigree reporting and supply-chain control including pharmacies.
1. Federal Register Notice of August 2, 1973 (38 FR 20750) 2. Federal Register Notice of October 17, 1980 (45 FR 69043, 69044) 3. Federal Register Notice of March 5, 1996 (61 FR 8760)
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