NDC Package 81425-003-10 Lumo Booz Hangover Companiion

Chininum Arsenicosum,Natrum Phosphoricum,Nux Voomica,Vespa Crabro Tablet, Chewable Oral - 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:
81425-003-10
Package Description:
180 TABLET, CHEWABLE in 1 BOTTLE
Product Code:
Proprietary Name:
Lumo Booz Hangover Companiion
Non-Proprietary Name:
Chininum Arsenicosum, Natrum Phosphoricum, Nux Voomica, Vespa Crabro
Substance Name:
Quinine Arsenite; Sodium Phosphate, Dibasic, Heptahydrate; Strychnos Nux-vomica Seed; Vespa Crabro
Usage Information:
Uses* Temporarily Relieves Minor and Occasional:• headache • hyperacidity • heartburn • sour belching • gas • nausea• symptoms of hangover • motion sickness • irritable • dizziness
11-Digit NDC Billing Format:
81425000310
Product Type:
Human Otc Drug
Labeler Name:
Applied Bioenergetics, Llc
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:
    10-15-2023
    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 81425-003-10?

    The NDC Packaged Code 81425-003-10 is assigned to a package of 180 tablet, chewable in 1 bottle of Lumo Booz Hangover Companiion, a human over the counter drug labeled by Applied Bioenergetics, Llc. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 81425-003 included in the NDC Directory?

    Yes, Lumo Booz Hangover Companiion with product code 81425-003 is active and included in the NDC Directory. The product was first marketed by Applied Bioenergetics, Llc on October 15, 2023 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 81425-003-10?

    The 11-digit format is 81425000310. 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 5-3-2 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
    5-3-281425-003-105-4-281425-0003-10