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  5. NDC Package Code: 51048-202-25 Odorono Antiperspirant And Deodorant Roll-on Powder

NDC Package 51048-202-25 Odorono Antiperspirant And Deodorant Roll-on Powder

Aluminum Chlorohydrate Liquid 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:
51048-202-25
Package Description:
74 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
51048-202
Proprietary Name:
Odorono Antiperspirant And Deodorant Roll-on Powder
Non-Proprietary Name:
Aluminum Chlorohydrate
Substance Name:
Aluminum Chlorohydrate
Usage Information:
Use: Reduces underarm wetness
11-Digit NDC Billing Format:
51048020225
Product Type:
Human Otc Drug
Labeler Name:
Omega & Delta Co
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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):
  • ALUMINUM CHLOROHYDRATE 20 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    part350
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    05-08-2006
    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 51048-202-25?

    The NDC Packaged Code 51048-202-25 is assigned to a package of 74 ml in 1 bottle, with applicator of Odorono Antiperspirant And Deodorant Roll-on Powder, a human over the counter drug labeled by Omega & Delta Co. The product's dosage form is liquid and is administered via topical form.

    Is NDC 51048-202 included in the NDC Directory?

    Yes, Odorono Antiperspirant And Deodorant Roll-on Powder with product code 51048-202 is active and included in the NDC Directory. The product was first marketed by Omega & Delta Co on May 08, 2006 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 51048-202-25?

    The 11-digit format is 51048020225. 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
    5-3-251048-202-255-4-251048-0202-25