1. Home
  2. Labeler Index
  3. Anicare Pharmaceuticals Pvt. Ltd.
  4. 47046-176
  5. NDC Package Code: 47046-176-01 Lucky Supersoft Maximum Strength

NDC Package 47046-176-01 Lucky Supersoft 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:
47046-176-01
Package Description:
14 g in 1 TUBE
Product Code:
47046-176
Proprietary Name:
Lucky Supersoft Maximum Strength
Usage Information:
■ for itching of skin irritation, inflammation and rashes: ■ 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: ask a doctor for external anal and genital itching, adults: ■ when practical, clean the affected area with mild soap and water and rinse thoroughly ■ gently dry by patting or blotting with toilet tissue or a soft cloth before applying ■ apply to affected area not more than 3 to 4 times daily ■ children under 12 years of age: ask a doctor
11-Digit NDC Billing Format:
47046017601
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:
    Anicare Pharmaceuticals Pvt. Ltd.
    Sample Package:
    No
    Start Marketing Date:
    01-31-2015
    Listing Expiration Date:
    12-31-2021
    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 47046-176-01?

    The NDC Packaged Code 47046-176-01 is assigned to a package of 14 g in 1 tube of Lucky Supersoft Maximum Strength, labeled by Anicare Pharmaceuticals Pvt. Ltd.. The product's dosage form is and is administered via form.

    Is NDC 47046-176 included in the NDC Directory?

    No, Lucky Supersoft Maximum Strength with product code 47046-176 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Anicare Pharmaceuticals Pvt. Ltd. on January 31, 2015 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 47046-176-01?

    The 11-digit format is 47046017601. 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
    5-3-247046-176-015-4-247046-0176-01