NDC Package 82157-005-10 Nioxin Scalp Recovery Soothing Serum

Pyrithione Zinc 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:
82157-005-10
Package Description:
100 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Nioxin Scalp Recovery Soothing Serum
Non-Proprietary Name:
Pyrithione Zinc
Substance Name:
Pyrithione Zinc
Usage Information:
Useshelps prevent recurrence of flaking and itching associated with dandruff.
11-Digit NDC Billing Format:
82157000510
NDC to RxNorm Crosswalk:
  • RxCUI: 1245090 - zinc pyrithione 0.1 % Topical Solution
  • RxCUI: 1245090 - zinc pyrithione 1 MG/ML Topical Solution
  • RxCUI: 1245095 - NIOXIN Scalp Recovery 0.1 % Topical Solution
  • RxCUI: 1245095 - zinc pyrithione 1 MG/ML Topical Solution [Nioxin]
  • RxCUI: 1245095 - Nioxin 0.1 % Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Wella Operations Us Llc
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    M032
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    12-01-2022
    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 82157-005-10?

    The NDC Packaged Code 82157-005-10 is assigned to a package of 100 ml in 1 bottle, plastic of Nioxin Scalp Recovery Soothing Serum, a human over the counter drug labeled by Wella Operations Us Llc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 82157-005 included in the NDC Directory?

    Yes, Nioxin Scalp Recovery Soothing Serum with product code 82157-005 is active and included in the NDC Directory. The product was first marketed by Wella Operations Us Llc on December 01, 2022 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 82157-005-10?

    The 11-digit format is 82157000510. 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
    5-3-282157-005-105-4-282157-0005-10