NDC Package 50845-0264-1 Snore Defense

Antimonium Tartaricum,Carbo Vegetabilis,Grindelia (robusta),Lung Suis,Mucosa Nasalis - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
50845-0264-1
Package Description:
30 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Snore Defense
Non-Proprietary Name:
Antimonium Tartaricum, Carbo Vegetabilis, Grindelia (robusta), Lung Suis, Mucosa Nasalis Suis, Nux Vomica, Sambucus Nigra, Sticta Pulmonaria, Teucrium Marum
Substance Name:
Activated Charcoal; Antimony Potassium Tartrate; Grindelia Hirsutula Flowering Top; Lobaria Pulmonaria; Sambucus Nigra Flowering Top; Strychnos Nux-vomica Seed; Sus Scrofa Lung; Sus Scrofa Nasal Mucosa; Teucrium Marum
Usage Information:
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.
11-Digit NDC Billing Format:
50845026401
Product Type:
Human Otc Drug
Labeler Name:
Liddell Laboratories
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    03-10-2020
    End Marketing Date:
    12-17-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 50845-0264-1?

    The NDC Packaged Code 50845-0264-1 is assigned to a package of 30 ml in 1 bottle, spray of Snore Defense, a human over the counter drug labeled by Liddell Laboratories. The product's dosage form is spray and is administered via oral form.

    Is NDC 50845-0264 included in the NDC Directory?

    Yes, Snore Defense with product code 50845-0264 is active and included in the NDC Directory. The product was first marketed by Liddell Laboratories on March 10, 2020.

    What is the 11-digit format for NDC 50845-0264-1?

    The 11-digit format is 50845026401. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-150845-0264-15-4-250845-0264-01