NDC Package 52358-0002-1 Supraderm

White Petrolatum,Lanolin Cream 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:
52358-0002-1
Package Description:
113 g in 1 JAR
Product Code:
Proprietary Name:
Supraderm
Non-Proprietary Name:
White Petrolatum, Lanolin
Substance Name:
Lanolin; Petrolatum
Usage Information:
Apply liberally to affected area of the skin as needed.
11-Digit NDC Billing Format:
52358000201
NDC to RxNorm Crosswalk:
  • RxCUI: 1593062 - petrolatum 30 % / lanolin 15 % Topical Cream
  • RxCUI: 1593062 - lanolin 150 MG/ML / petrolatum 300 MG/ML Topical Cream
  • RxCUI: 1593067 - SUPRADERM 30 % / 15 % Topical Cream
  • RxCUI: 1593067 - lanolin 150 MG/ML / petrolatum 300 MG/ML Topical Cream [Supraderm]
  • RxCUI: 1593067 - Supraderm (lanolin 15 % / petrolatum 30 % ) Topical Cream
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Olen Skin Care Corporation
    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):
    Sample Package:
    No
    FDA Application Number:
    M016
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-17-2014
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    52358-0002-2340 g in 1 JAR
    52358-0002-3454 g in 1 JAR

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52358-0002-1?

    The NDC Packaged Code 52358-0002-1 is assigned to a package of 113 g in 1 jar of Supraderm, a human over the counter drug labeled by Olen Skin Care Corporation. The product's dosage form is cream and is administered via topical form.

    Is NDC 52358-0002 included in the NDC Directory?

    Yes, Supraderm with product code 52358-0002 is active and included in the NDC Directory. The product was first marketed by Olen Skin Care Corporation on October 17, 2014 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 52358-0002-1?

    The 11-digit format is 52358000201. 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 5-4-1 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
    5-4-152358-0002-15-4-252358-0002-01