NDC Package 63736-921-18 Sucrets Vapor Cherry

Dyclonine Hydrochloride And Menthol Lozenge Oral - 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:
63736-921-18
Package Description:
18 LOZENGE in 1 CANISTER
Product Code:
Proprietary Name:
Sucrets Vapor Cherry
Non-Proprietary Name:
Dyclonine Hydrochloride And Menthol
Substance Name:
Dyclonine Hydrochloride; Menthol
Usage Information:
Do not use more than directedadults and children 4 years of age and older: allow lozenge to dissolve slowly in mouth. May be repeated every 2 hours as needed or as directed by a dentist and doctor.children under 4 years of age: ask a dentist and doctor
11-Digit NDC Billing Format:
63736092118
NDC to RxNorm Crosswalk:
  • RxCUI: 2052919 - dyclonine hydrochloride 2 MG / menthol 6 MG Oral Lozenge
  • RxCUI: 2052925 - Sucrets Sore Throat 2 MG / 6 MG Oral Lozenge
  • RxCUI: 2052925 - dyclonine hydrochloride 2 MG / menthol 6 MG Oral Lozenge [Sucrets Sore Throat]
  • RxCUI: 2052925 - Sucrets Sore Throat (dyclonine hydrochloride 2 MG / menthol 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.
  • Sample Package:
    No
    FDA Application Number:
    part356
    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:
    07-28-2009
    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 63736-921-18?

    The NDC Packaged Code 63736-921-18 is assigned to a package of 18 lozenge in 1 canister of Sucrets Vapor Cherry, 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 63736-921 included in the NDC Directory?

    Yes, Sucrets Vapor Cherry with product code 63736-921 is active and included in the NDC Directory. The product was first marketed by Insight Pharmaceuticals Llc on July 28, 2009 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 63736-921-18?

    The 11-digit format is 63736092118. 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
    5-3-263736-921-185-4-263736-0921-18