61152-196 NDC - SNORE STOP EXTINGUISHER THROAT ()

Drug Information

  • Product NDC: 61152-196
  • Proprietary Name: Snore Stop Extinguisher Throat
  • Non Proprietary Name:
  • Active Ingredient(s): 6 [hp_X]/4.5mL ATROPA BELLADONNA; 6 [hp_X]/4.5mL EPHEDRA DISTACHYA FLOWERING TWIG; 6 [hp_X]/4.5mL GOLDENSEAL; 12 [hp_X]/4.5mL HISTAMINE DIHYDROCHLORIDE; 6 [hp_X]/4.5mL POTASSIUM DICHROMATE; 6 [hp_X]/4.5mL STRYCHNOS NUX-VOMICA SEED; 6 [hp_X]/4.5mL TEUCRIUM MARUM
  • Administration Route(s):
  • Dosage Form(s):
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Green Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/15/2012

Package Information

No. Package Code Package Description Billing Unit
161152-196-064.5 mL in 1 BOTTLE, SPRAY (61152-196-06)
261152-196-1818 mL in 1 BOTTLE, SPRAY (61152-196-18)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61152-196The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMESnore Stop Extinguisher ThroatThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/15/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEGreen PharmaceuticalsName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC61152-196The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMESnore Stop Extinguisher ThroatThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/28/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEGreen Pharmaceuticals IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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