Livita Children Liquid
NDC Package 59088-660-16

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Livita Children (folate, multivitamin) liquids is livita™ 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 formulation utilizes a liquid delivery system. Marketed by Puretek Corporation, this product is identified by NDC 59088-660.

Identification & Billing

NDC Package Code
59088-660-16
Package Description
237 mL in 1 BOTTLE
Product Code
59088-660
11-Digit Billing Format
59088066016
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
237 ML

Clinical Specifications

Proprietary Name
Livita Children
Non-Proprietary Name
Folate, Multivitamin
Substance Name
.alpha.-tocopherol Acetate, D-; Ascorbic Acid; Biotin; Calcium Citrate; Calcium Pantothenate; Cholecalciferol; Choline Bitartrate; Inulin; Levomefolate Calcium; Magnesium Citrate; Methylcobalamin; Niacinamide; Pyridoxine Hydrochloride; Riboflavin; Thiamine Mononitrate; Vitamin A Acetate; Zinc Picolinate
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Livita™ 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 a licensed healthcare practitioner to ensure that any potential for nutritional deficiency is addressed in a manner that supports the individual's overall health and wellbeing.

Regulatory & Marketing

Labeler Name
Puretek Corporation
Product Type
Human Prescription Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
12-18-2023
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 59088-660-16 identifies a specific commercial package of 237 ml in 1 bottle of Livita Children, a human prescription drug labeled by Puretek Corporation. This product is billed per "ML" milliliter and contains an estimated amount of 237 billable units per package. This liquid is formulated for oral use and contains .alpha.-tocopherol acetate, d-; ascorbic acid; biotin; calcium citrate; calcium pantothenate; cholecalciferol; choline bitartrate; inulin; levomefolate calcium; magnesium citrate; methylcobalamin; niacinamide; pyridoxine hydrochloride; riboflavin; thiamine mononitrate; vitamin a acetate; zinc picolinate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Puretek Corporation on December 18, 2023. The current certification is valid through December 31, 2026.

How is this Puretek Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59088066016. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 237 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
59088-660-16
11-Digit CMS (5-4-2)
59088-0660-16

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.