NDC Package 69968-0475-4 Aveeno Anti-itch Concentrated

Zinc Oxide,Ferric Oxide Red,And Pramoxine Hydrochloride Lotion 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:
69968-0475-4
Package Description:
118 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Aveeno Anti-itch Concentrated
Non-Proprietary Name:
Zinc Oxide, Ferric Oxide Red, And Pramoxine Hydrochloride
Substance Name:
Ferric Oxide Red; Pramoxine Hydrochloride; Zinc Oxide
Usage Information:
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.
11-Digit NDC Billing Format:
69968047504
NDC to RxNorm Crosswalk:
  • RxCUI: 1233698 - calamine 3 % / pramoxine HCl 1 % Topical Lotion
  • RxCUI: 1233698 - calamine 30 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Lotion
  • RxCUI: 1233698 - calamine 3 % / pramoxine hydrochloride 1 % Topical Lotion
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer Inc.
    Dosage Form:
    Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
    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.
  • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    03-01-2019
    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 69968-0475-4?

    The NDC Packaged Code 69968-0475-4 is assigned to a package of 118 ml in 1 bottle of Aveeno Anti-itch Concentrated, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is lotion and is administered via topical form.

    Is NDC 69968-0475 included in the NDC Directory?

    Yes, Aveeno Anti-itch Concentrated with product code 69968-0475 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on March 01, 2019 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 69968-0475-4?

    The 11-digit format is 69968047504. 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
    5-4-169968-0475-45-4-269968-0475-04