1. Home
  2. Labeler Index
  3. Nucare Pharmaceuticals, Inc.
  4. 68071-3197
  5. NDC Package Code: 68071-3197-1 Hydrocortisone With Aloe Maximum Strength

NDC Package 68071-3197-1 Hydrocortisone With Aloe Maximum Strength

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
68071-3197-1
Package Description:
1 g in 1 TUBE
Product Code:
68071-3197
Proprietary Name:
Hydrocortisone With Aloe Maximum Strength
Usage Information:
Adults and children 2 years of age and older  • apply to affected area not more than 3 to 4 times daily Children under 2 years of age  • do not use, consult a doctor   For external anal itching Adults: when practical, clean the affected area with mild soap and warm water, rinse thoroughly, gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product Children under 12 years of age: consult a doctor
11-Digit NDC Billing Format:
68071319701
NDC to RxNorm Crosswalk:
  • RxCUI: 106258 - hydrocortisone 1 % Topical Cream
  • RxCUI: 106258 - hydrocortisone 10 MG/ML Topical Cream
  • RxCUI: 106258 - hydrocortisone 1 % (as hydrocortisone acetate 1.2 % ) Topical Cream
  • RxCUI: 106258 - hydrocortisone 1 GM per 100 GM Topical Cream
    • Labeler Name:
    Nucare Pharmaceuticals, Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-08-1998
    Listing Expiration Date:
    12-31-2020
    Exclude Flag:
    I
    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 68071-3197-1?

    The NDC Packaged Code 68071-3197-1 is assigned to a package of 1 g in 1 tube of Hydrocortisone With Aloe Maximum Strength, labeled by Nucare Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

    Is NDC 68071-3197 included in the NDC Directory?

    No, Hydrocortisone With Aloe Maximum Strength with product code 68071-3197 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Nucare Pharmaceuticals, Inc. on July 08, 1998 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68071-3197-1?

    The 11-digit format is 68071319701. 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
    5-4-168071-3197-15-4-268071-3197-01