NDC Package 57483-410-13 Xyralid Hemorrhoidal

Hemorrhoidal Suppositories Suppository Rectal - 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:
57483-410-13
Package Description:
4 BLISTER PACK in 1 CARTON / 24 g in 1 BLISTER PACK (57483-410-12)
Product Code:
Proprietary Name:
Xyralid Hemorrhoidal
Non-Proprietary Name:
Hemorrhoidal Suppositories
Substance Name:
Cocoa Butter; Phenylephrine Hydrochloride
Usage Information:
-Adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe.  Gently dry by patting or blotting with a toilet tissue or a soft cloth.-remove the wrapper before inserting into the rectum.-insert one suppository into the rectum up to 4 times daily, especially at night, in the morning or after each bowel movement.-Children under 12 years of age: consult a doctor
11-Digit NDC Billing Format:
57483041013
NDC to RxNorm Crosswalk:
  • RxCUI: 1438497 - cocoa butter 88.4 % / phenylephrine HCl 0.25 % Rectal Suppository
  • RxCUI: 1438497 - cocoa butter 0.884 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Innovus Pharmaceuticals, Inc.
    Dosage Form:
    Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.
    Administration Route(s):
  • Rectal - Administration to the rectum.
  • Sample Package:
    No
    FDA Application Number:
    part346
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    03-25-2018
    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 57483-410-13?

    The NDC Packaged Code 57483-410-13 is assigned to a package of 4 blister pack in 1 carton / 24 g in 1 blister pack (57483-410-12) of Xyralid Hemorrhoidal, a human over the counter drug labeled by Innovus Pharmaceuticals, Inc.. The product's dosage form is suppository and is administered via rectal form.

    Is NDC 57483-410 included in the NDC Directory?

    Yes, Xyralid Hemorrhoidal with product code 57483-410 is active and included in the NDC Directory. The product was first marketed by Innovus Pharmaceuticals, Inc. on March 25, 2018 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 57483-410-13?

    The 11-digit format is 57483041013. 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
    5-3-257483-410-135-4-257483-0410-13