Snorestop Spray
NDC Package 61152-600-59

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

Package Information

Snorestop (nux vomica, belladonna, hydrastis canadensis, kali bichromicum, teucrium marum, histaminum hydrochloricum, laurocerasus, cinchona, stramonium) sprays is adults and children 12 years of age and older: Spray twice under the tongue and twice in the back of the throat at bedtime. This formulation utilizes a spray delivery system. Marketed by Green Pharmaceuticals Inc, this product is identified by NDC 61152-600.

Identification & Billing

NDC Package Code
61152-600-59
Package Description
59 mL in 1 BOTTLE, SPRAY
Product Code
61152-600
11-Digit Billing Format
61152060059

Clinical Specifications

Proprietary Name
Snorestop
Non-Proprietary Name
Nux Vomica, Belladonna, Hydrastis Canadensis, Kali Bichromicum, Teucrium Marum, Histaminum Hydrochloricum, Laurocerasus, Cinchona, Stramonium
Substance Name
Atropa Belladonna; Cinchona Bark; Datura Stramonium; Histamine Dihydrochloride; Hydrastis Canadensis Whole; Potassium Dichromate; Prunus Laurocerasus Leaf; Strychnos Nux-vomica Seed; Teucrium Marum
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
Adults and children 12 years of age and older: Spray twice under the tongue and twice in the back of the throat at bedtime. Use 30 mins apart from any food, water, or medicine.Initially, depress pump until primed.Please allow 3-5 days for initial treatment.Consult a physician for use in children under 12 years of age.Use additionally as needed, up to 4 times per day.

Regulatory & Marketing

Labeler Name
Green Pharmaceuticals Inc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-19-2025
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 61152-600-59 identifies a specific commercial package of 59 ml in 1 bottle, spray of Snorestop, a human over the counter drug labeled by Green Pharmaceuticals Inc. This spray is formulated for oral use and contains atropa belladonna; cinchona bark; datura stramonium; histamine dihydrochloride; hydrastis canadensis whole; potassium dichromate; prunus laurocerasus leaf; strychnos nux-vomica seed; teucrium marum 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 Green Pharmaceuticals Inc on June 19, 2025. The current certification is valid through December 31, 2026.

How is this Green Pharmaceuticals Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61152060059. 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)
61152-600-59
11-Digit CMS (5-4-2)
61152-0600-59

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