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  5. NDC Package Code: 48201-015-18 Angidol Raspberry

NDC Package 48201-015-18 Angidol Raspberry

Benzocaine,Menthol Lozenge Oral - 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:
48201-015-18
Package Description:
18 LOZENGE in 1 CARTON
Product Code:
48201-015
Proprietary Name:
Angidol Raspberry
Non-Proprietary Name:
Benzocaine, Menthol
Substance Name:
Benzocaine; Menthol
Usage Information:
Adults and children 5 years and older: allow 1 lozenge to dissolve slowly in mouth. May be repeated every two hours as necessary or as directed by a doctorchildren under 5 years: do not use
11-Digit NDC Billing Format:
48201001518
NDC to RxNorm Crosswalk:
  • RxCUI: 1658672 - Angidol 15 MG / 2.6 MG Oral Lozenge
  • RxCUI: 1658672 - benzocaine 15 MG / menthol 2.6 MG Oral Lozenge [Angidol]
  • RxCUI: 1658672 - Angidol (benzocaine 15 MG / menthol 2.6 MG) Oral Lozenge
  • RxCUI: 858664 - benzocaine 15 MG / menthol 2.6 MG Oral Lozenge
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Grandall Distributing, Llc
    Dosage Form:
    Lozenge - A solid preparation containing one or more medicaments, usually in a flavored, sweetened base which is intended to dissolve or disintegrate slowly in the mouth. A lollipop is a lozenge on a stick.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • BENZOCAINE 15 mg/1
  • MENTHOL 2.6 mg/1
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-24-2023
    Listing Expiration Date:
    12-31-2025
    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 48201-015-18?

    The NDC Packaged Code 48201-015-18 is assigned to a package of 18 lozenge in 1 carton of Angidol Raspberry, a human over the counter drug labeled by Grandall Distributing, Llc. The product's dosage form is lozenge and is administered via oral form.

    Is NDC 48201-015 included in the NDC Directory?

    Yes, Angidol Raspberry with product code 48201-015 is active and included in the NDC Directory. The product was first marketed by Grandall Distributing, Llc on March 24, 2023 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 48201-015-18?

    The 11-digit format is 48201001518. 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
    5-3-248201-015-185-4-248201-0015-18