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  5. NDC Package Code: 69379-001-03 Simanix

NDC Package 69379-001-03 Simanix

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:
69379-001-03
Package Description:
120 g in 1 BOTTLE
Product Code:
69379-001
Proprietary Name:
Simanix
Usage Information:
INDICATIONS For the temporary relief of minor pain of muscles and joints associated with: ArthritisSimple Backache Strains Sprains Bruises DIRECTIONSAdults and children over 18 years:Apply generously to affected areaMassage into painful area until thoroughly absorbed into skinRepeat as necessary, not more than 3-4 times daily.Wash hands with soap and water immediately after use.Children 18 years or younger: ask a doctorStore at 20°-25°C (68°-77 °F). Avoid direct sunlight.
11-Digit NDC Billing Format:
69379000103
NDC to RxNorm Crosswalk:
  • RxCUI: 1656333 - capsaicin 0.0375 % / menthol 3 % / histamine dihydrochloride 0.035 % Topical Cream
  • RxCUI: 1656333 - capsaicin 0.375 MG/ML / histamine dihydrochloride 0.35 MG/ML / menthol 30 MG/ML Topical Cream
  • RxCUI: 1656333 - capsaicin 0.0375 % / histamine dihydrochloride 0.035 % / menthol 3 % Topical Cream
    • Labeler Name:
    Home Aide Diagnostics, Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-08-2015
    Listing Expiration Date:
    12-31-2017
    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 69379-001-03?

    The NDC Packaged Code 69379-001-03 is assigned to a package of 120 g in 1 bottle of Simanix, labeled by Home Aide Diagnostics, Inc.. The product's dosage form is and is administered via form.

    Is NDC 69379-001 included in the NDC Directory?

    No, Simanix with product code 69379-001 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Home Aide Diagnostics, Inc. on July 08, 2015 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69379-001-03?

    The 11-digit format is 69379000103. 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
    5-3-269379-001-035-4-269379-0001-03