Advance Plus Spray
NDC Package 70964-0001-1

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

Package Information

Advance Plus (carduus marianus, cynara scolymus, solidago virgaurea, taraxacum officinale, benzoicum acidum, berberis vulgaris, bryonia (alba), cantharis, carduus benedictus, ceanothus americanus, chelidonium majus, chionanthus virginica, cinchona officinalis, dioscorea villosa, dolichos pruriens, iris versicolor, juniperus communis, nux vomica, ptelea trifoliata, uricum acidum) sprays is formulated for liver, kidney and colon functions and for symptoms associated with toxic conditions.**These statements have not been evaluated by the Food and Drug Administration. This formulation utilizes a spray delivery system. Marketed by Vitaminmed, Llc, this product is identified by NDC 70964-0001.

Identification & Billing

NDC Package Code
70964-0001-1
Package Description
30 mL in 1 BOTTLE, SPRAY
Product Code
70964-0001
11-Digit Billing Format
70964000101

Clinical Specifications

Proprietary Name
Advance Plus
Non-Proprietary Name
Carduus Marianus, Cynara Scolymus, Solidago Virgaurea, Taraxacum Officinale, Benzoicum Acidum, Berberis Vulgaris, Bryonia (alba), Cantharis, Carduus Benedictus, Ceanothus Americanus, Chelidonium Majus, Chionanthus Virginica, Cinchona Officinalis, Dioscorea Villosa, Dolichos Pruriens, Iris Versicolor, Juniperus Communis, Nux Vomica, Ptelea Trifoliata, Uricum Acidum
Substance Name
Benzoic Acid; Berberis Vulgaris Root Bark; Bryonia Alba Root; Ceanothus Americanus Leaf; Centaurea Benedicta; Chelidonium Majus Whole; Chionanthus Virginicus Bark; Cinchona Officinalis Bark; Cynara Scolymus Leaf; Dioscorea Villosa Tuber; Iris Versicolor Root; Juniper Berry; Lytta Vesicatoria; Milk Thistle; Mucuna Pruriens Fruit Trichome; Ptelea Trifoliata Bark; Solidago Virgaurea Flowering Top; Strychnos Nux-vomica Seed; Taraxacum Officinale; Uric Acid
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Formulated for liver, kidney and colon functions and for symptoms associated with toxic conditions.**These statements have not been evaluated by the Food and Drug Administration.  This product is not intended to diagnose, treat, cure, or prevent any disease. Formulated for liver, kidney and colon functions and for symptoms associated with toxic conditions.**These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Regulatory & Marketing

Labeler Name
Vitaminmed, 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
12-08-2016
Listing Expiration
12-31-2027
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 70964-0001-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Advance Plus, a human over the counter drug labeled by Vitaminmed, Llc. This spray is formulated for oral use and contains benzoic acid; berberis vulgaris root bark; bryonia alba root; ceanothus americanus leaf; centaurea benedicta; chelidonium majus whole; chionanthus virginicus bark; cinchona officinalis bark; cynara scolymus leaf; dioscorea villosa tuber; iris versicolor root; juniper berry; lytta vesicatoria; milk thistle; mucuna pruriens fruit trichome; ptelea trifoliata bark; solidago virgaurea flowering top; strychnos nux-vomica seed; taraxacum officinale; uric acid 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 Vitaminmed, Llc on December 08, 2016. The current certification is valid through December 31, 2027.

How is this Vitaminmed, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70964000101. 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 (5-4-1)
70964-0001-1
11-Digit CMS (5-4-2)
70964-0001-01

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