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  5. NDC Package Code: 24286-1532-7 Tincture Merthiolate

NDC Package 24286-1532-7 Tincture Merthiolate

Benzalkonium Chloride Tincture 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:
24286-1532-7
Package Description:
30 mL in 1 BOTTLE
Product Code:
24286-1532
Proprietary Name:
Tincture Merthiolate
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Adults and children 2 years of age and older: clean the affected area apply a small amount of this product to the area using the enclosed applicator or a cotton-tipped applicator 1 to 3 times daily _ may be covered with a sterile bandage (let dry first) children under 2 years, ask a doctor
11-Digit NDC Billing Format:
24286153207
NDC to RxNorm Crosswalk:
  • RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
  • RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Dlc Laboratories, Inc
    Dosage Form:
    Tincture - An alcoholic or hydroalcoholic solution prepared from vegetable materials or from chemical substances.
    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):
  • BENZALKONIUM CHLORIDE 1.3 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-22-2013
    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 24286-1532-7?

    The NDC Packaged Code 24286-1532-7 is assigned to a package of 30 ml in 1 bottle of Tincture Merthiolate, a human over the counter drug labeled by Dlc Laboratories, Inc. The product's dosage form is tincture and is administered via topical form.

    Is NDC 24286-1532 included in the NDC Directory?

    Yes, Tincture Merthiolate with product code 24286-1532 is active and included in the NDC Directory. The product was first marketed by Dlc Laboratories, Inc on March 22, 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 24286-1532-7?

    The 11-digit format is 24286153207. 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 5-4-1 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
    5-4-124286-1532-75-4-224286-1532-07