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  5. NDC Package Code: 82160-127-01 Aquax-h

NDC Package 82160-127-01 Aquax-h

Hydrocortisone Butyrate Cream 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:
82160-127-01
Package Description:
1 TUBE in 1 CARTON / 30 g in 1 TUBE
Product Code:
82160-127
Proprietary Name:
Aquax-h
Non-Proprietary Name:
Hydrocortisone Butyrate
Substance Name:
Hydrocortisone Butyrate
Usage Information:
This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Hydrocortisone butyrate reduces the swelling, itching, and redness that can occur in these types of conditions. The topical solution is used to treat severe dandruff (seborrheic dermatitis). This medication is a medium-strength corticosteroid.
11-Digit NDC Billing Format:
82160012701
NDC to RxNorm Crosswalk:
  • RxCUI: 1370770 - hydrocortisone butyrate 0.1 % Topical Cream
  • RxCUI: 1370770 - hydrocortisone butyrate 1 MG/ML Topical Cream
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Pella Pharmaceuticals Co. Ltd
    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):
  • HYDROCORTISONE BUTYRATE 30 mg/30g
    • Pharmacologic Class(es):
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    03-16-2015
    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 82160-127-01?

    The NDC Packaged Code 82160-127-01 is assigned to a package of 1 tube in 1 carton / 30 g in 1 tube of Aquax-h, a human prescription drug labeled by Pella Pharmaceuticals Co. Ltd. The product's dosage form is cream and is administered via topical form.

    Is NDC 82160-127 included in the NDC Directory?

    Yes, Aquax-h with product code 82160-127 is active and included in the NDC Directory. The product was first marketed by Pella Pharmaceuticals Co. Ltd on March 16, 2015 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 82160-127-01?

    The 11-digit format is 82160012701. 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
    5-3-282160-127-015-4-282160-0127-01