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  5. NDC Package Code: 68400-203-18 Hemox A

NDC Package 68400-203-18 Hemox A

Aluminum Chloride Solution Dental - 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:
68400-203-18
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
68400-203
Proprietary Name:
Hemox A
Non-Proprietary Name:
Aluminum Chloride
Substance Name:
Aluminum Chloride
Usage Information:
This medication is used to help control excessive sweating.
11-Digit NDC Billing Format:
68400020318
NDC to RxNorm Crosswalk:
  • RxCUI: 244613 - aluminum chloride 25 % Topical Solution
  • RxCUI: 244613 - aluminum chloride 250 MG/ML Topical Solution
  • RxCUI: 672193 - Hemox A 25 % Topical Solution
  • RxCUI: 672193 - aluminum chloride 250 MG/ML Topical Solution [Hemox A]
  • RxCUI: 672193 - Hemox A 250 MG/ML Topical Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Mycone Dental Supply Co., Inc Dba Keystone Industries And Deepak Products Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Dental - Administration to a tooth or teeth.
    • Active Ingredient(s):
  • ALUMINUM CHLORIDE 7500 mg/30mL
    • 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:
    01-15-2013
    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 68400-203-18?

    The NDC Packaged Code 68400-203-18 is assigned to a package of 30 ml in 1 bottle, glass of Hemox A, a human prescription drug labeled by Mycone Dental Supply Co., Inc Dba Keystone Industries And Deepak Products Inc.. The product's dosage form is solution and is administered via dental form.

    Is NDC 68400-203 included in the NDC Directory?

    Yes, Hemox A with product code 68400-203 is active and included in the NDC Directory. The product was first marketed by Mycone Dental Supply Co., Inc Dba Keystone Industries And Deepak Products Inc. on January 15, 2013 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 68400-203-18?

    The 11-digit format is 68400020318. 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
    5-3-268400-203-185-4-268400-0203-18