NDC 50845-0251 Snore Defense

Antimonium Tartaricum, Carbo Vegetabilis, Grindelia (robusta), Lung Suis, Mucosa Nasalis Suis, Nux Vomica, Quebracho, Sticta Pulmonaria, Teucrium Marum

  1. Labeler Index
  2. Liddell Laboratories
  3. NDC: 50845-0251 Snore Defense

NDC Product Code 50845-0251

NDC CODE: 50845-0251

Proprietary Name: Snore Defense 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.
Non-Proprietary Name: Antimonium Tartaricum, Carbo Vegetabilis, Grindelia (robusta), Lung Suis, Mucosa Nasalis Suis, Nux Vomica, Quebracho, Sticta Pulmonaria, Teucrium Marum 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.

NDC Code Structure

  • 50845 - Liddell Laboratories

NDC 50845-0251-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Snore Defense with NDC 50845-0251 is a 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.

Labeler Name: Liddell Laboratories

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Snore Defense Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
  • ANTIMONY POTASSIUM TARTRATE 200 [hp_C]/mL
  • ACTIVATED CHARCOAL 12 [hp_X]/mL
  • GRINDELIA HIRSUTULA FLOWERING TOP 200 [hp_C]/mL
  • SUS SCROFA LUNG 6 [hp_X]/mL
  • SUS SCROFA NASAL MUCOSA 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • ASPIDOSPERMA QUEBRACHO-BLANCO BARK 3 [hp_X]/mL
  • LOBARIA PULMONARIA 200 [hp_C]/mL
  • TEUCRIUM MARUM 3 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

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.

Labeler Name: Liddell Laboratories
Labeler Code: 50845
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.
Start Marketing Date: 04-02-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Snore Defense Product Label Images

Snore Defense Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

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 LABORATORIESWOODBINE, IA 51579WWW.LIDDELL.NET 1-800-460-7733

Package Label Display:

ORAL SPRAYSLIDDELLLABORATORIESEST. 199457SN-Snore DefenseHOMEOPATHIC1.0 FL. OZ. (30 ML)

* Please review the disclaimer below.