Vivacity Liquid
NDC Package 27281-039-64

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

Package Information

Vivacity (alfalfa, arnica montana, avena sativa, galium aparine, hepar suis, hypericum perforatum, korean ginseng, oleum animale, pituitary suis, rhus toxicodendron, rna, thuja occidentalis) liquids is a human otc drug administered via oral route. This formulation utilizes a liquid delivery system. Marketed by Sunway Biotech Llc, this product is identified by NDC 27281-039.

Identification & Billing

NDC Package Code
27281-039-64
Package Description
30 mL in 1 BOTTLE, SPRAY
Product Code
27281-039
11-Digit Billing Format
27281003964

Clinical Specifications

Proprietary Name
Vivacity
Non-Proprietary Name
Alfalfa, Arnica Montana, Avena Sativa, Galium Aparine, Hepar Suis, Hypericum Perforatum, Korean Ginseng, Oleum Animale, Pituitary Suis, Rhus Toxicodendron, Rna, Thuja Occidentalis
Substance Name
Alfalfa; Arnica Montana; Asian Ginseng; Avena Sativa Flowering Top; Cervus Elaphus Horn Oil; Galium Aparine; Hypericum Perforatum; Pork Liver; Saccharomyces Cerevisiae Rna; Sus Scrofa Pituitary Gland; Thuja Occidentalis Leafy Twig; Toxicodendron Pubescens Leaf
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)

Regulatory & Marketing

Labeler Name
Sunway Biotech Llc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
02-05-2018
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 27281-039-64 identifies a specific commercial package of 30 ml in 1 bottle, spray of Vivacity, a human over the counter drug labeled by Sunway Biotech Llc. This liquid is formulated for oral use and contains alfalfa; arnica montana; asian ginseng; avena sativa flowering top; cervus elaphus horn oil; galium aparine; hypericum perforatum; pork liver; saccharomyces cerevisiae rna; sus scrofa pituitary gland; thuja occidentalis leafy twig; toxicodendron pubescens leaf 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 Sunway Biotech Llc on February 05, 2018. The current certification is valid through December 31, 2026.

How is this Sunway Biotech Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 27281003964. 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)
27281-039-64
11-Digit CMS (5-4-2)
27281-0039-64

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