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  5. NDC Package Code: 73519-001-30 Babysons

NDC Package 73519-001-30 Babysons

Dexpanthenol Ointment Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
73519-001-30
Package Description:
1 TUBE in 1 BOX / 30 g in 1 TUBE
Product Code:
73519-001
Proprietary Name:
Babysons
Non-Proprietary Name:
Dexpanthenol
Substance Name:
Dexpanthenol
Usage Information:
Change wet and soiled diapers promptly.Cleanse the diaper area and allow to dryApply product liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.
11-Digit NDC Billing Format:
73519000130
NDC to RxNorm Crosswalk:
  • RxCUI: 249792 - dexpanthenol 5 % Topical Ointment
  • RxCUI: 249792 - dexpanthenol 0.05 MG/MG Topical Ointment
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Laboratorios Quimica Son's, S.a. De C.v
    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):
  • DEXPANTHENOL 50 mg/g
    • Sample Package:
    No
    FDA Application Number:
    M016
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-15-2020
    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.

    Frequently Asked Questions

    What is NDC 73519-001-30?

    The NDC Packaged Code 73519-001-30 is assigned to a package of 1 tube in 1 box / 30 g in 1 tube of Babysons, a human over the counter drug labeled by Laboratorios Quimica Son's, S.a. De C.v. The product's dosage form is ointment and is administered via topical form.

    Is NDC 73519-001 included in the NDC Directory?

    Yes, Babysons with product code 73519-001 is active and included in the NDC Directory. The product was first marketed by Laboratorios Quimica Son's, S.a. De C.v on June 15, 2020 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 73519-001-30?

    The 11-digit format is 73519000130. 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
    5-3-273519-001-305-4-273519-0001-30