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  5. NDC Package Code: 69423-615-11 Bodewell Eczema Daily Soothing

NDC Package 69423-615-11 Bodewell Eczema Daily Soothing

Colloidal Oatmeal Spray 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:
69423-615-11
Package Description:
118 mL in 1 BOTTLE, SPRAY
Product Code:
69423-615
Proprietary Name:
Bodewell Eczema Daily Soothing
Non-Proprietary Name:
Colloidal Oatmeal
Substance Name:
Oatmeal
Usage Information:
Apply as needed
11-Digit NDC Billing Format:
69423061511
NDC to RxNorm Crosswalk:
  • RxCUI: 1552199 - colloidal oatmeal 1 % Lotion Spray
  • RxCUI: 1552199 - colloidal oatmeal 10 MG/ML Topical Spray
    • Product Type:
    Human Otc Drug
    Labeler Name:
    The Procter & Gamble Manufacturing Company
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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):
  • OATMEAL 1 g/100mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Grain Proteins - [EXT]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
    • Sample Package:
    No
    FDA Application Number:
    M016
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-15-2022
    End Marketing Date:
    04-30-2024
    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 69423-615-11?

    The NDC Packaged Code 69423-615-11 is assigned to a package of 118 ml in 1 bottle, spray of Bodewell Eczema Daily Soothing, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is spray and is administered via topical form.

    Is NDC 69423-615 included in the NDC Directory?

    Yes, Bodewell Eczema Daily Soothing with product code 69423-615 is active and included in the NDC Directory. The product was first marketed by The Procter & Gamble Manufacturing Company on February 15, 2022.

    What is the 11-digit format for NDC 69423-615-11?

    The 11-digit format is 69423061511. 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
    5-3-269423-615-115-4-269423-0615-11