NDC Package 65923-564-20 Coralite Pain Relief

Camphor,Menthol,Methyl Salicylate Patch 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:
65923-564-20
Package Description:
20 PATCH in 1 PACKAGE / 1 g in 1 PATCH
Product Code:
Proprietary Name:
Coralite Pain Relief
Non-Proprietary Name:
Camphor, Menthol, Methyl Salicylate
Substance Name:
Camphor (synthetic); Menthol; Methyl Salicylate
Usage Information:
Directionsadults and children 12 years of age and over:clean and dry affected arearemove patch from filmapply to affected area not more than 3 to 4 times dailyremove patch from the skin after at most 8 hours' applicationchildren under 12 years of age: consult a doctor
11-Digit NDC Billing Format:
65923056420
NDC to RxNorm Crosswalk:
  • RxCUI: 853260 - camphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated Patch
  • RxCUI: 853260 - camphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 MG/MG Medicated Patch
  • Product Type:
    Human Otc Drug
    Labeler Name:
    United Exchange Corp.
    Dosage Form:
    Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
    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:
    04-12-2016
    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 65923-564-20?

    The NDC Packaged Code 65923-564-20 is assigned to a package of 20 patch in 1 package / 1 g in 1 patch of Coralite Pain Relief, a human over the counter drug labeled by United Exchange Corp.. The product's dosage form is patch and is administered via topical form.

    Is NDC 65923-564 included in the NDC Directory?

    Yes, Coralite Pain Relief with product code 65923-564 is active and included in the NDC Directory. The product was first marketed by United Exchange Corp. on April 12, 2016 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 65923-564-20?

    The 11-digit format is 65923056420. 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
    5-3-265923-564-205-4-265923-0564-20