NDC Package 62795-4004-9 Reboost

Apis Mellifera,Atropa Belladonna,Zinc Gluconate,Baptisia Tinctoria Root,Ulmus Rubra - 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:
62795-4004-9
Package Description:
1 BOTTLE, SPRAY in 1 CARTON / 20 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Reboost
Non-Proprietary Name:
Apis Mellifera, Atropa Belladonna, Zinc Gluconate, Baptisia Tinctoria Root, Ulmus Rubra Bark, Sulfur, Zinc Acetate Anhydrous, Vincetoxicum Hirundinaria Root And Cairina Moschata Heart/liver
Substance Name:
Apis Mellifera; Atropa Belladonna; Baptisia Tinctoria Root; Cairina Moschata Heart/liver Autolysate; Calendula Officinalis Flowering Top; Echinacea Purpurea; Goldenseal; Phytolacca Americana Root; Plantago Major; Sage; Sulfur; Ulmus Rubra Bark; Vincetoxicum Hirundinaria Root; Zinc Acetate Anhydrous; Zinc Gluconate
Usage Information:
Directions: Adults and children 12 years and older: 2 sprays onto affected area every 2-4 hours. Do not exceed 24 sprays in  24 hours.For Children under 12 years:  consult your health professional.
11-Digit NDC Billing Format:
62795400409
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Product Type:
Human Otc Drug
Labeler Name:
Medinatura
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:
    02-05-2020
    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 62795-4004-9?

    The NDC Packaged Code 62795-4004-9 is assigned to a package of 1 bottle, spray in 1 carton / 20 ml in 1 bottle, spray of Reboost, a human over the counter drug labeled by Medinatura. The product's dosage form is spray and is administered via oral form.

    Is NDC 62795-4004 included in the NDC Directory?

    Yes, Reboost with product code 62795-4004 is active and included in the NDC Directory. The product was first marketed by Medinatura on February 05, 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 NDC billing unit for package 62795-4004-9?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 62795-4004-9?

    The 11-digit format is 62795400409. 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
    5-4-162795-4004-95-4-262795-4004-09