NDC Package 69676-0028-1 Genexa Motion Sickness Relief

Bryonia Alba,Cinnamonum,Cocculus Indica,Colchicum Autumnale,Iris Versicolor,Kali - 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:
69676-0028-1
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Genexa Motion Sickness Relief
Non-Proprietary Name:
Bryonia Alba, Cinnamonum, Cocculus Indica, Colchicum Autumnale, Iris Versicolor, Kali Carbonicum, Nux Moschata, Staphysagria, Tabacum, Zingiber Officinale
Substance Name:
Anamirta Cocculus Seed; Bryonia Alba Whole; Cinnamon; Colchicum Autumnale Bulb; Delphinium Staphisagria Seed; Ginger; Iris Versicolor Root; Nutmeg; Potassium Carbonate; Tobacco Leaf
Usage Information:
Uses*addresses the following symptoms associated with motion sickness:nauseavomitingdizziness
11-Digit NDC Billing Format:
69676002801
Product Type:
Human Otc Drug
Labeler Name:
Genexa Inc.
Dosage Form:
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
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:
    01-21-2020
    Listing Expiration Date:
    12-31-2024
    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 69676-0028-1?

    The NDC Packaged Code 69676-0028-1 is assigned to a package of 1 bottle, plastic in 1 carton / 60 tablet, chewable in 1 bottle, plastic of Genexa Motion Sickness Relief, a human over the counter drug labeled by Genexa Inc.. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 69676-0028 included in the NDC Directory?

    Yes, Genexa Motion Sickness Relief with product code 69676-0028 is active and included in the NDC Directory. The product was first marketed by Genexa Inc. on January 21, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69676-0028-1?

    The 11-digit format is 69676002801. 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
    5-4-169676-0028-15-4-269676-0028-01