Hcg Formula Spray
NDC Package 57520-0181-1

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

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Hcg Formula (foeniculum vulgare, fucus vesiculosus, lecithin, ammonium carbonicum, caulophyllum thalictroides, galium aparine, lac defloratum, phosphorus, phytolacca decandra, rubus idaeus, abrotanum,) sprays is iNDICATIONS:  May help to release stored fat for consumption by the body. This formulation utilizes a spray delivery system. Marketed by Apotheca Company, this product is identified by NDC 57520-0181.

Identification & Billing

NDC Package Code
57520-0181-1
Package Description
30 mL in 1 BOTTLE, SPRAY
Product Code
57520-0181
11-Digit Billing Format
57520018101

Clinical Specifications

Proprietary Name
Hcg Formula
Non-Proprietary Name
Foeniculum Vulgare, Fucus Vesiculosus, Lecithin, Ammonium Carbonicum, Caulophyllum Thalictroides, Galium Aparine, Lac Defloratum, Phosphorus, Phytolacca Decandra, Rubus Idaeus, Abrotanum,
Substance Name
Fennel Seed; Fucus Vesiculosus; Lecithin, Soybean; Ammonium Carbonate; Caulophyllum Thalictroides Root; Galium Aparine; Skim Milk; Phosphorus; Phytolacca Americana Root; Artemisia Abrotanum Flowering Top; Semecarpus Anacardium Juice; Arsenic Trioxide; Barium Chloride Dihydrate; Helleborus Niger Root; Strychnos Ignatii Seed; Lycopodium Clavatum Spore; Niacinamide; Claviceps Purpurea Sclerotium; Sus Scrofa Thymus; Sus Scrofa Thyroid; Ammonium Bromide; Antimony Trisulfide; Calcium Arsenate; Manganese; Oyster Shell Calcium Carbonate, Crude; Tribasic Calcium Phosphate; Silicon Dioxide; Human Chorionic Gonadotropin; Rubus Idaeus Leaf
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
INDICATIONS:  May help to release stored fat for consumption by the body.

Regulatory & Marketing

Labeler Name
Apotheca Company
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
12-30-2010
End Marketing Date
08-31-2026
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 57520-0181-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Hcg Formula, a human over the counter drug labeled by Apotheca Company. This spray is formulated for oral use and contains fennel seed; fucus vesiculosus; lecithin, soybean; ammonium carbonate; caulophyllum thalictroides root; galium aparine; skim milk; phosphorus; phytolacca americana root; artemisia abrotanum flowering top; semecarpus anacardium juice; arsenic trioxide; barium chloride dihydrate; helleborus niger root; strychnos ignatii seed; lycopodium clavatum spore; niacinamide; claviceps purpurea sclerotium; sus scrofa thymus; sus scrofa thyroid; ammonium bromide; antimony trisulfide; calcium arsenate; manganese; oyster shell calcium carbonate, crude; tribasic calcium phosphate; silicon dioxide; human chorionic gonadotropin; rubus idaeus 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 Apotheca Company on December 30, 2010.

How is this Apotheca Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 57520018101. 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)
57520-0181-1
11-Digit CMS (5-4-2)
57520-0181-01

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