Appetrol 20 Liquid
NDC Package 87115-0001-1

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

Package Information

Appetrol 20 (fucus vesiculosus, chelidonium majus, kali phosphoricum, lycopodium clavatum, natrum muriaticum, quercus glandium spiritus, quercus robur, nux vomica, phytolacca decandra, ornithogalum umbellatum, agnus castus, berberis aquifolium, berberis vulgaris, saccharum officinale, solidago virgaurea, calcarea carbonica, carbo vegetabilis, magnesia phosphorica, natrum phosphoricum, sinapis arvensis, flos, ubidecarenonum, graphites, hypophysis suis, placenta totalis suis, hypothalamus (bovine)) liquids is 0.5 mL (approximately 10-15 drops) three times a day. This formulation utilizes a liquid delivery system. Marketed by Carbalor Llc, this product is identified by NDC 87115-0001.

Identification & Billing

NDC Package Code
87115-0001-1
Package Description
60 mL in 1 BOTTLE, DROPPER
Product Code
87115-0001
11-Digit Billing Format
87115000101

Clinical Specifications

Proprietary Name
Appetrol 20
Non-Proprietary Name
Fucus Vesiculosus, Chelidonium Majus, Kali Phosphoricum, Lycopodium Clavatum, Natrum Muriaticum, Quercus Glandium Spiritus, Quercus Robur, Nux Vomica, Phytolacca Decandra, Ornithogalum Umbellatum, Agnus Castus, Berberis Aquifolium, Berberis Vulgaris, Saccharum Officinale, Solidago Virgaurea, Calcarea Carbonica, Carbo Vegetabilis, Magnesia Phosphorica, Natrum Phosphoricum, Sinapis Arvensis, Flos, Ubidecarenonum, Graphites, Hypophysis Suis, Placenta Totalis Suis, Hypothalamus (bovine)
Substance Name
Activated Charcoal; Berberis Aquifolium Root Bark; Berberis Vulgaris Root Bark; Bos Taurus Hypothalamus; Chaste Tree Fruit; Chelidonium Majus Whole; Dibasic Potassium Phosphate; Fucus Vesiculosus; Graphite; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Ornithogalum Umbellatum Whole; Oyster Shell Calcium Carbonate, Crude; Phytolacca Americana Root; Quercus Robur Nut; Quercus Robur Twig Bark; Sinapis Arvensis Flowering/fruiting Top; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate; Solidago Virgaurea Flowering Top; Strychnos Nux-vomica Seed; Sucrose; Sus Scrofa Pituitary Gland; Sus Scrofa Placenta; Ubidecarenone
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
0.5 mL (approximately 10-15 drops) three times a day. Let rest under the tongue for 60-120 seconds, then swallow. Avoid eating or drinking 15 minutes before and after taking drops. Consult a physician for use in children under 12 years of age.

Regulatory & Marketing

Labeler Name
Carbalor 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
03-12-2026
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 87115-0001-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Appetrol 20, a human over the counter drug labeled by Carbalor Llc. This liquid is formulated for oral use and contains activated charcoal; berberis aquifolium root bark; berberis vulgaris root bark; bos taurus hypothalamus; chaste tree fruit; chelidonium majus whole; dibasic potassium phosphate; fucus vesiculosus; graphite; lycopodium clavatum spore; magnesium phosphate, dibasic trihydrate; ornithogalum umbellatum whole; oyster shell calcium carbonate, crude; phytolacca americana root; quercus robur nut; quercus robur twig bark; sinapis arvensis flowering/fruiting top; sodium chloride; sodium phosphate, dibasic, heptahydrate; solidago virgaurea flowering top; strychnos nux-vomica seed; sucrose; sus scrofa pituitary gland; sus scrofa placenta; ubidecarenone 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 Carbalor Llc on March 12, 2026. The current certification is valid through December 31, 2027.

How is this Carbalor Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87115000101. 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)
87115-0001-1
11-Digit CMS (5-4-2)
87115-0001-01

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