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  5. NDC Package Code: 63736-567-18 Sucrets

NDC Package 63736-567-18 Sucrets

Dyclonine Hcl,Menthol,And Pectin 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:
63736-567-18
Package Description:
18 LOZENGE in 1 CAN
Product Code:
63736-567
Proprietary Name:
Sucrets
Non-Proprietary Name:
Dyclonine Hcl, Menthol, And Pectin
Substance Name:
Dyclonine Hydrochloride; Menthol; Pectin
Usage Information:
Do not use more than directedadults and children 4 years of age and older: Dissolve 1 lozenge slowly in the mouth. May be repeated every 2 hours as needed or as directed by a doctor or dentistchildren under 4 years of age: consult a doctor or dentist
11-Digit NDC Billing Format:
63736056718
NDC to RxNorm Crosswalk:
  • RxCUI: 1992531 - dyclonine HCl 2 MG / menthol 5 MG / pectin 6 MG Oral Lozenge
  • RxCUI: 1992531 - dyclonine hydrochloride 2 MG / menthol 5 MG / pectin 6 MG Oral Lozenge
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Insight Pharmaceuticals 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):
  • DYCLONINE HYDROCHLORIDE 2 mg/1
  • MENTHOL 5 mg/1
  • PECTIN 6 mg/1
    • Sample Package:
    No
    FDA Application Number:
    M022
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-04-2014
    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 63736-567-18?

    The NDC Packaged Code 63736-567-18 is assigned to a package of 18 lozenge in 1 can of Sucrets, a human over the counter drug labeled by Insight Pharmaceuticals Llc. The product's dosage form is lozenge and is administered via oral form.

    Is NDC 63736-567 included in the NDC Directory?

    Yes, Sucrets with product code 63736-567 is active and included in the NDC Directory. The product was first marketed by Insight Pharmaceuticals Llc on November 04, 2014 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 63736-567-18?

    The 11-digit format is 63736056718. 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
    5-3-263736-567-185-4-263736-0567-18