NDC Package 62795-1042-2 Reboost

Aconitum Napellus,Bryonia Alba Root,Eupatorium Perfoliatum Flowering - 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:
62795-1042-2
Package Description:
1 BOTTLE in 1 CARTON / 60 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Reboost
Non-Proprietary Name:
Aconitum Napellus, Bryonia Alba Root, Eupatorium Perfoliatum Flowering Top, Goldenseal, Lachesis Muta Venom, Phosphorus, Vincetoxicum Hirundinaria Root, Zinc Gluconate, Zinc Acetate Anhydrous, Cairina Moschata Heart/liver Autolysate, Ipecac, Sulfur And Influenza A Virus A/singapore/6/86 (h1n1) Antigen (heat Inactivated)
Substance Name:
Aconitum Napellus; Bryonia Alba Root; Cairina Moschata Heart/liver Autolysate; Eupatorium Perfoliatum Flowering Top; Goldenseal; Influenza A Virus A/singapore/6/86 (h1n1) Antigen (heat Inactivated); Ipecac; Lachesis Muta Venom; Phosphorus; Sulfur; Vincetoxicum Hirundinaria Root; Zinc Acetate Anhydrous; Zinc Gluconate
Usage Information:
Directions: For max absorption, dissolve undertongue. Can be chewed and swallowed. Adults andchildren 12 years and older: 2 tablets every 4 hours.Do not exceed 12 tablets per 24 hours. Children 4 to11 years: 1-2 tablets every 4 hours. Do not exceed12 tablets per 24 hours. For children under 4 years,consult your health professional.
11-Digit NDC Billing Format:
62795104202
Product Type:
Human Otc Drug
Labeler Name:
Medinatura Inc.
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
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:
    02-19-2020
    End Marketing Date:
    04-30-2025
    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 62795-1042-2?

    The NDC Packaged Code 62795-1042-2 is assigned to a package of 1 bottle in 1 carton / 60 tablet in 1 bottle of Reboost, a human over the counter drug labeled by Medinatura Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 62795-1042 included in the NDC Directory?

    Yes, Reboost with product code 62795-1042 is active and included in the NDC Directory. The product was first marketed by Medinatura Inc. on February 19, 2020.

    What is the 11-digit format for NDC 62795-1042-2?

    The 11-digit format is 62795104202. 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
    5-4-162795-1042-25-4-262795-1042-02