PRECAUTIONS SECTION.
Precaution Section. Folate doses above 0.1 mg daily may obscure pernicious anemia, in that hematologic remission can occur while neurological manifestations remain progressive. There is potential danger in administering folate to patients with undiagnosed anemia since folate may obscure the diagnosis of pernicious anemia by alleviating the hematologic manifestations of the disease while allowing the neurologic complications to progress. This may result in severe nervous system damage before the correct diagnosis is made. Adequate doses of vitamin B12 may prevent, halt, or improve the neurologic changes caused by pernicious anemia.The patients medical conditions and consumption of other drugs, herbs, and/or supplements should be considered.For use on the order of licensed healthcare practitioner. Call your doctor about side effects. To report side effects, call PureTek Corporation at 1-877-921-7873 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Citing DrugCentral © 2026. License
STORAGE AND HANDLING SECTION.
STORAGE:. Do not use if bottle seal is broken. KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. Store at controlled room temperature 20 to 25C (68 to 77F). [See USP]. Protect from light and moisture and avoid excessive heat.
Citing DrugCentral © 2026. License
ADVERSE REACTIONS SECTION.
Adverse Reactions:. Folate: Allergic sensitizations have been reported following both oral and parenteral administration of folate. Adverse reactions have been reported with specific vitamins and minerals but generally at levels substantially higher than those contained herein. However, allergic, and idiosyncratic reactions are possible at lower levels.
Citing DrugCentral © 2026. License
CONTRAINDICATIONS SECTION.
Contraindications:. This product is contraindicated in patients with known hypersensitivity to any of its ingredients.
Citing DrugCentral © 2026. License
DESCRIPTION SECTION.
DESCRIPTION:. Active Ingredients: Amount Per Serving: Vitamin (as Retinyl Acetate).................................... 900 mcg RAE Vitamin (as Ascorbic Acid)............................................... 200 mg Vitamin D3 (as Cholecalciferol)............................................ 10 mcg Vitamin (as D-Alpha Tocopheryl Acetate)............................ 30 mg Thiamin (as Thiamine Mononitrate)...................................... 1.2 mg Riboflavin ............................................................................. 1.3 mg Niacin (as Niacinamide)........................................................... mg Vitamin B6 (as Pyridoxine Hydrochloride)............................ 1.7 mg Folate (as L-5-Methyltetrahydrofolate calcium salt)...1700 mcg DFE (1000 mcg of L-5-Methylfolate) Vitamin B12 (as Methylcobalamin and Hydroxocobalamin)...2.4 mcg Biotin (as D-Biotin)............................................................... 30 mcg Pantothenic Acid (as D-Calcium Pantothenate)........................ mg Choline (as Choline Bitartrate)............................................. 200 mg Calcium (as Calcium Citrate)................................................ 200 mg Magnesium (as Magnesium Citrate).................................... 100 mg Zinc (as Zinc Picolinate)........................................................... mg Inulin (as Helianthus Tuberosus Root Extract)..................... 500 mg Other Ingredients: Aqua (Water), Organic Agave Syrup, Carrageenan, Citrus Extract, Flavor, Glycerin, Hydroxocobalamin Acetate, Potassium Sorbate, Organic Stevia Rebaudiana Leaf Extract.
Citing DrugCentral © 2026. License
DOSAGE & ADMINISTRATION SECTION.
Dosage and Administration:. Livita(TM) Liquid Multivitamin for Adults: The usual adult dose is tablespoon (15 mL) daily.
Citing DrugCentral © 2026. License
HOW SUPPLIED SECTION.
How Supplied:. Livita(TM) Liquid Multivitamin for Adults is available in 16 fl.oz. bottle with an NDC of 59088-659-31. All prescription substitutions using this product shall be pursuant to state statutes as applicable. This is not an Orange Book product.
Citing DrugCentral © 2026. License
INDICATIONS & USAGE SECTION.
INDICATIONS AND USAGE:. Livita(TM) liquid is indicated to provide significant amounts of essential vitamins and minerals, including Vitamins A, C, D, E, thiamine, riboflavin, niacin, vitamin B6, vitamin B12, folate, calcium, magnesium, and zinc, to supplement the diet. This comprehensive nutrient profile helps prevent nutritional deficiencies of these vitamins and minerals, ensuring that the specific dietary needs of adults and children are met to support overall health, energy, and vitality. The product is specially formulated to target common vitamin and mineral gaps in adults, thus promoting optimal health, immune function, bone strength, and metabolic balance. It is intended to be used under the guidance of licensed healthcare practitioner to ensure that any potential for nutritional deficiency is addressed in manner that supports the individuals overall health and wellbeing.
Citing DrugCentral © 2026. License
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.
Livita(TM). Manufactured in the USA by:PureTek Corporation Panorama City, CA 91402 Questions Call toll-free: 1-877-921-7873 Label.
Citing DrugCentral © 2026. License
WARNINGS SECTION.
WARNING:. In case of accidental overdose, seek professional assistance or contact Poison Control Center immediately.. Precaution Section. Folate doses above 0.1 mg daily may obscure pernicious anemia, in that hematologic remission can occur while neurological manifestations remain progressive. There is potential danger in administering folate to patients with undiagnosed anemia since folate may obscure the diagnosis of pernicious anemia by alleviating the hematologic manifestations of the disease while allowing the neurologic complications to progress. This may result in severe nervous system damage before the correct diagnosis is made. Adequate doses of vitamin B12 may prevent, halt, or improve the neurologic changes caused by pernicious anemia.The patients medical conditions and consumption of other drugs, herbs, and/or supplements should be considered.For use on the order of licensed healthcare practitioner. Call your doctor about side effects. To report side effects, call PureTek Corporation at 1-877-921-7873 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. Adverse Reactions:. Folate: Allergic sensitizations have been reported following both oral and parenteral administration of folate. Adverse reactions have been reported with specific vitamins and minerals but generally at levels substantially higher than those contained herein. However, allergic, and idiosyncratic reactions are possible at lower levels.
Citing DrugCentral © 2026. License