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  5. NDC Package Code: 55910-330-24 Dg Health Medicated Anti-itch Analgesic

NDC Package 55910-330-24 Dg Health Medicated Anti-itch Analgesic

Menthol,Unspecified Form And Pramoxine Hydrochloride Cream Topical - 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:
55910-330-24
Package Description:
1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code:
55910-330
Proprietary Name:
Dg Health Medicated Anti-itch Analgesic
Non-Proprietary Name:
Menthol, Unspecified Form And Pramoxine Hydrochloride
Substance Name:
Menthol, Unspecified Form; Pramoxine Hydrochloride
Usage Information:
Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: ask a doctor
11-Digit NDC Billing Format:
55910033024
NDC to RxNorm Crosswalk:
  • RxCUI: 1116155 - menthol 1 % / pramoxine HCl 1 % Topical Cream
  • RxCUI: 1116155 - menthol 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream
  • RxCUI: 1116155 - menthol 1 % / pramoxine hydrochloride 1 % Topical Cream
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Dolgencorp, Llc
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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.
    • Active Ingredient(s):
  • MENTHOL, UNSPECIFIED FORM 10 mg/g
  • PRAMOXINE HYDROCHLORIDE 10 mg/g
    • Sample Package:
    No
    FDA Application Number:
    part347
    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:
    01-02-2008
    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 55910-330-24?

    The NDC Packaged Code 55910-330-24 is assigned to a package of 1 tube in 1 carton / 28 g in 1 tube of Dg Health Medicated Anti-itch Analgesic, a human over the counter drug labeled by Dolgencorp, Llc. The product's dosage form is cream and is administered via topical form.

    Is NDC 55910-330 included in the NDC Directory?

    Yes, Dg Health Medicated Anti-itch Analgesic with product code 55910-330 is active and included in the NDC Directory. The product was first marketed by Dolgencorp, Llc on January 02, 2008 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 55910-330-24?

    The 11-digit format is 55910033024. 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
    5-3-255910-330-245-4-255910-0330-24