NDC Package 70242-125-05 Veneno De Abeja Aceite De Vibora Brand

Methyl Salicylate Ointment 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:
70242-125-05
Package Description:
150 g in 1 JAR
Product Code:
Proprietary Name:
Veneno De Abeja Aceite De Vibora Brand
Non-Proprietary Name:
Methyl Salicylate
Substance Name:
Methyl Salicylate
Usage Information:
adults and children 12 years of age or older: apply generously 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:
70242012505
NDC to RxNorm Crosswalk:
  • RxCUI: 1101920 - methyl salicylate 10.5 % Topical Ointment
  • RxCUI: 1101920 - methyl salicylate 0.105 MG/MG Topical Ointment
  • RxCUI: 1117110 - VENENO DE ABEJA ACEITE DE VIBORA BRAND 10.5 % Topical Ointment
  • RxCUI: 1117110 - methyl salicylate 0.105 MG/MG Topical Ointment [Veneno de Abeja Aceite de Vibora]
  • RxCUI: 1117110 - Veneno de Abeja Aceite de Vibora 0.105 MG/MG Topical Ointment
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Dannso Corp./d.b.a. Essential Products
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >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:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-01-2015
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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 70242-125-05?

    The NDC Packaged Code 70242-125-05 is assigned to a package of 150 g in 1 jar of Veneno De Abeja Aceite De Vibora Brand, a human over the counter drug labeled by Dannso Corp./d.b.a. Essential Products. The product's dosage form is ointment and is administered via topical form.

    Is NDC 70242-125 included in the NDC Directory?

    Yes, Veneno De Abeja Aceite De Vibora Brand with product code 70242-125 is active and included in the NDC Directory. The product was first marketed by Dannso Corp./d.b.a. Essential Products on May 01, 2015 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 70242-125-05?

    The 11-digit format is 70242012505. 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
    5-3-270242-125-055-4-270242-0125-05