Heilen Liquid
NDC Package 70719-0003-1

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

Package Information

Heilen (galium aparine, agnus castus, apis mellifica, capsicum annuum, chelidonium majus, taraxacum officinale, urtica dioica, xanthoxylum fraxineum, fucus vesiculosus, kali phosphoricum, magnesia phosphorica, natrum phosphoricum, sarsaparilla (smilax regelii), ubidecarenonum, calcarea carbonica, graphites, lycopodium clavatum, anacardium orientale, colchicum autumnale, nux vomica, phytolacca decandra, pulsatilla (pratensis), histaminum hydrochloricum) liquids is for temporary relief of symptoms related to increased appetite, regulation of fat metabolism, sluggish metabolism, headache, and fatigue.****These statements are based upon homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Heilen, this product is identified by NDC 70719-0003.

Identification & Billing

NDC Package Code
70719-0003-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
70719-0003
11-Digit Billing Format
70719000301

Clinical Specifications

Proprietary Name
Heilen
Non-Proprietary Name
Galium Aparine, Agnus Castus, Apis Mellifica, Capsicum Annuum, Chelidonium Majus, Taraxacum Officinale, Urtica Dioica, Xanthoxylum Fraxineum, Fucus Vesiculosus, Kali Phosphoricum, Magnesia Phosphorica, Natrum Phosphoricum, Sarsaparilla (smilax Regelii), Ubidecarenonum, Calcarea Carbonica, Graphites, Lycopodium Clavatum, Anacardium Orientale, Colchicum Autumnale, Nux Vomica, Phytolacca Decandra, Pulsatilla (pratensis), Histaminum Hydrochloricum
Substance Name
Apis Mellifera; Capsicum; Chaste Tree Fruit; Chelidonium Majus Whole; Colchicum Autumnale Bulb; Dibasic Potassium Phosphate; Fucus Vesiculosus; Galium Aparine Whole; Graphite; Histamine Dihydrochloride; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Oyster Shell Calcium Carbonate, Crude; Phytolacca Americana Root; Pulsatilla Pratensis Whole; Semecarpus Anacardium Juice; Smilax Ornata Root; Sodium Phosphate, Dibasic, Heptahydrate; Strychnos Nux-vomica Seed; Taraxacum Officinale; Ubidecarenone; Urtica Dioica Whole; Zanthoxylum Americanum Bark
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
For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, sluggish metabolism, headache, and fatigue.****These statements are based upon homeopathic principles. They have not been approved by the Food and Drug Administration. For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, sluggish metabolism, headache, and fatigue.****These statements are based upon homeopathic principles. They have not been approved by the Food and Drug Administration.

Regulatory & Marketing

Labeler Name
Heilen
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
01-21-2022
End Marketing Date
02-04-2027
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 70719-0003-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Heilen, a human over the counter drug labeled by Heilen. This liquid is formulated for oral use and contains apis mellifera; capsicum; chaste tree fruit; chelidonium majus whole; colchicum autumnale bulb; dibasic potassium phosphate; fucus vesiculosus; galium aparine whole; graphite; histamine dihydrochloride; lycopodium clavatum spore; magnesium phosphate, dibasic trihydrate; oyster shell calcium carbonate, crude; phytolacca americana root; pulsatilla pratensis whole; semecarpus anacardium juice; smilax ornata root; sodium phosphate, dibasic, heptahydrate; strychnos nux-vomica seed; taraxacum officinale; ubidecarenone; urtica dioica whole; zanthoxylum americanum bark 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 Heilen on January 21, 2022.

How is this Heilen product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70719000301. 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)
70719-0003-1
11-Digit CMS (5-4-2)
70719-0003-01

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