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  5. NDC Package Code: 34666-201-01 Hemorrhoidex

NDC Package 34666-201-01 Hemorrhoidex

Ratanhia,Hamamelis Ointment Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
34666-201-01
Package Description:
1 TUBE in 1 CARTON / 28.35 g in 1 TUBE
Product Code:
34666-201
Proprietary Name:
Hemorrhoidex
Non-Proprietary Name:
Ratanhia, Hamamelis
Substance Name:
Hamamelis Virginiana Root Bark/stem Bark; Krameria Lappacea Root
Usage Information:
Adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe.  Apply generously to affected area up to 2 times daily, especially at night, in the morning or after each bowel movementreapply if neededchildren under 12 years of age, consult a physician
11-Digit NDC Billing Format:
34666020101
Product Type:
Human Otc Drug
Labeler Name:
Nartex Laboratorios Homeopaticos Sa De Cv
Dosage Form:
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 1 [hp_X]/28.35g
  • KRAMERIA LAPPACEA ROOT 3 [hp_X]/28.35g
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    04-17-2015
    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 34666-201-01?

    The NDC Packaged Code 34666-201-01 is assigned to a package of 1 tube in 1 carton / 28.35 g in 1 tube of Hemorrhoidex, a human over the counter drug labeled by Nartex Laboratorios Homeopaticos Sa De Cv. The product's dosage form is ointment and is administered via topical form.

    Is NDC 34666-201 included in the NDC Directory?

    Yes, Hemorrhoidex with product code 34666-201 is active and included in the NDC Directory. The product was first marketed by Nartex Laboratorios Homeopaticos Sa De Cv on April 17, 2015 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 34666-201-01?

    The 11-digit format is 34666020101. 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
    5-3-234666-201-015-4-234666-0201-01