NDC Package 90107-1280-1 After Bite Kids

Sodium Bicarbonate Cream 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:
90107-1280-1
Package Description:
1 TUBE in 1 BOX / 20 g in 1 TUBE
Product Code:
Proprietary Name:
After Bite Kids
Non-Proprietary Name:
Sodium Bicarbonate
Substance Name:
Sodium Bicarbonate
Usage Information:
Use cap to puncture safety seal.Adults and children 2 years and older for use as a cream, apply to the affected area of the skin as needed or as directed by a doctor Children under 2 years ask a doctor
11-Digit NDC Billing Format:
90107128001
NDC to RxNorm Crosswalk:
  • RxCUI: 1722238 - sodium bicarbonate 5 % Topical Cream
  • RxCUI: 1722238 - sodium bicarbonate 50 MG/ML Topical Cream
  • RxCUI: 1722238 - NaHCO3 50 MG/ML Topical Cream
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Adventure Ready Brands
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 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:
    M016
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    09-01-2020
    Listing Expiration Date:
    12-31-2025
    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 90107-1280-1?

    The NDC Packaged Code 90107-1280-1 is assigned to a package of 1 tube in 1 box / 20 g in 1 tube of After Bite Kids, a human over the counter drug labeled by Adventure Ready Brands. The product's dosage form is cream and is administered via topical form.

    Is NDC 90107-1280 included in the NDC Directory?

    Yes, After Bite Kids with product code 90107-1280 is active and included in the NDC Directory. The product was first marketed by Adventure Ready Brands on September 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 90107-1280-1?

    The 11-digit format is 90107128001. 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
    5-4-190107-1280-15-4-290107-1280-01