NDC 50845-0251 Snore Defense
Antimonium Tartaricum, Carbo Vegetabilis, Grindelia (robusta), Lung Suis, Mucosa Nasal...

Product Information

What is NDC 50845-0251?

The NDC code 50845-0251 is assigned by the FDA to the product Snore Defense which is a human over the counter drug product labeled by Liddell Laboratories. The generic name of Snore Defense is antimonium tartaricum, carbo vegetabilis, grindelia (robusta), lung suis, mucosa nasalis suis, nux vomica, quebracho, sticta pulmonaria, teucrium marum. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 50845-0251-1 30 ml in 1 bottle, spray . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code50845-0251
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Snore Defense
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Antimonium Tartaricum, Carbo Vegetabilis, Grindelia (robusta), Lung Suis, Mucosa Nasalis Suis, Nux Vomica, Quebracho, Sticta Pulmonaria, Teucrium Marum
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Human Otc Drug
Dosage FormSpray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Liddell Laboratories
Labeler Code50845
Marketing Category What is the Marketing Category?
Product 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.
UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
04-02-2019
End Marketing Date What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
04-02-2024
Exclude Flag What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
N
NDC Code Structure

What are the uses for Snore Defense?


Product Packages

NDC Code 50845-0251-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

Product Details

What are Snore Defense Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Snore Defense Active Ingredients UNII Codes

  • ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
  • ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
  • ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
  • ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
  • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI)
  • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (Active Moiety)
  • SUS SCROFA LUNG (UNII: 7GL3G1COB3)
  • SUS SCROFA LUNG (UNII: 7GL3G1COB3) (Active Moiety)
  • SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY)
  • SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190)
  • ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190) (Active Moiety)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
  • TEUCRIUM MARUM (UNII: 10464S0TAA)
  • TEUCRIUM MARUM (UNII: 10464S0TAA) (Active Moiety)

Snore Defense Inactive Ingredients UNII Codes

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Snore Defense Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Active Ingredients:



Antimonium tartaricum 200C, Carbo vegetabilis 12X, Grindelia (Robusta) 200C, Lung suis 6X, Mucosa nasalis suis 6X, Nux vomica 12X, Quebracho 3X, Sticta pulmonaria 200C, Teucrium marum 3X.


Indications:



May help reduce the loudness and frequency of snoring and may promote a more restful night's sleep.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

May help reduce the loudness and frequency of snoring and may promote a more restful night's sleep.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.


Warnings:



Persons who have symptoms of sleep apnea should consult a doctor.

If pregnant or breast feeding, ask a doctor before use.

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.


Keep Out Of Reach Of Children:



Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.


Directions:



Adults: Spray twice under the tongue 3 times per day, with last dose at bedtime and additional doses whenever sleep is interrupted.


Inactive Ingredients:



Organic alcohol 20% v/v, Purified water.


Questions:



DIST. BY LIDDELL LABORATORIES

WOODBINE, IA 51579

WWW.LIDDELL.NET 1-800-460-7733


Package Label Display:



ORAL SPRAYS

LIDDELL

LABORATORIES

EST. 1994

57SN-

Snore Defense

HOMEOPATHIC

1.0 FL. OZ. (30 ML)


* Please review the disclaimer below.