NDC Package 71687-4000-1 Herpecin Pain Relief

Allantoin,Benzethonium Chloride,Lidocaine Hcl Gel Topical - 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:
71687-4000-1
Package Description:
1 TUBE in 1 CARTON / 4 g in 1 TUBE
Product Code:
Proprietary Name:
Herpecin Pain Relief
Non-Proprietary Name:
Allantoin, Benzethonium Chloride, Lidocaine Hcl
Substance Name:
Allantoin; Benzethonium Chloride; Lidocaine Hydrochloride Anhydrous
Usage Information:
Adults and children 12 years of age or older:■ clean the affected area■ apply externally to the lips 1 to 3 times dailychildren under 12 years of age: Ask a doctor
11-Digit NDC Billing Format:
71687400001
NDC to RxNorm Crosswalk:
  • RxCUI: 2566834 - allantoin 2 % / benzethonium chloride 0.2 % / lidocaine hydrochloride 4 % Oral Gel
  • RxCUI: 2566834 - allantoin 0.02 MG/MG / benzethonium chloride 0.002 MG/MG / lidocaine hydrochloride 0.04 MG/MG Oral Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Focus Consumer Healthcare, Llc
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    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.
  • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    06-11-2021
    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 71687-4000-1?

    The NDC Packaged Code 71687-4000-1 is assigned to a package of 1 tube in 1 carton / 4 g in 1 tube of Herpecin Pain Relief, a human over the counter drug labeled by Focus Consumer Healthcare, Llc. The product's dosage form is gel and is administered via topical form.

    Is NDC 71687-4000 included in the NDC Directory?

    Yes, Herpecin Pain Relief with product code 71687-4000 is active and included in the NDC Directory. The product was first marketed by Focus Consumer Healthcare, Llc on June 11, 2021 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 71687-4000-1?

    The 11-digit format is 71687400001. 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
    5-4-171687-4000-15-4-271687-4000-01