Snore Stop Extinguisher Throat Spray
NDC Package 61152-196-06
Package Information
Snore Stop Extinguisher Throat (atropa belladonna, ephedra distachya flowering twig, histamine dihydrochloride, goldenseal, potassium dichromate, strychnos nux-vomica seed, teucrium marum) sprays is children over 5 years of age and Adults.Shake before each use. This formulation utilizes a spray delivery system. Marketed by Green Pharmaceuticals Inc, this product is identified by NDC 61152-196.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 61152 - Green Pharmaceuticals Inc
- 61152-196 - Snore Stop Extinguisher Throat
- 61152-196-06 - 4.5 mL in 1 BOTTLE, SPRAY
- 61152-196 - Snore Stop Extinguisher Throat
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (61152-196). Click a package code to view its specific billing and regulatory data.
* 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 61152-196-06 identifies a specific commercial package of 4.5 ml in 1 bottle, spray of Snore Stop Extinguisher Throat, a human over the counter drug labeled by Green Pharmaceuticals Inc. This spray is formulated for oral use and contains atropa belladonna; ephedra distachya flowering twig; goldenseal; histamine dihydrochloride; potassium dichromate; 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 December 28, 2012. 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: 61152019606. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.