NDC Package 72968-0002-1 Herplex

Anatherum Muricatum,Clematis Erecta,Mezereum,Phytolacca Decandra,Ranunculus Bulbosus,Rhus - 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:
72968-0002-1
Package Description:
60 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Herplex
Non-Proprietary Name:
Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia
Substance Name:
Chrysopogon Zizanioides Root; Clematis Recta Flowering Top; Daphne Mezereum Bark; Phytolacca Americana Root; Ranunculus Bulbosus Whole; Sepia Officinalis Juice; Sodium Chloride; Thuja Occidentalis Leafy Twig; Toxicodendron Pubescens Leaf
Usage Information:
For use only after diagnoses by a physician, as follows:Cold Sores/Oral Herpes: Take 3 tablets immediately at the first sign of burning or itching and then 3 tablets three times daily until symptoms disappear.Genital Herpes: For severe genital herpes sufferers, take 3 to 5 tablets 3 times daily for prevention of outbreaks. If you have an outbreak that does not subside within 10 days, consult your doctor. For mild to moderate symptoms, take 3 tablets immediately at the first sign of burning or itching, and then 3 tablets three times daily until symptoms disappear. If symptoms do not subside within 10 days, consult your doctor.
11-Digit NDC Billing Format:
72968000201
Product Type:
Human Otc Drug
Labeler Name:
Nashco Products Llc
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:
    04-18-2019
    End Marketing Date:
    12-28-2026
    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 72968-0002-1?

    The NDC Packaged Code 72968-0002-1 is assigned to a package of 60 tablet in 1 bottle, plastic of Herplex, a human over the counter drug labeled by Nashco Products Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 72968-0002 included in the NDC Directory?

    Yes, Herplex with product code 72968-0002 is active and included in the NDC Directory. The product was first marketed by Nashco Products Llc on April 18, 2019.

    What is the 11-digit format for NDC 72968-0002-1?

    The 11-digit format is 72968000201. 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
    5-4-172968-0002-15-4-272968-0002-01