NDC Package 61734-030-03 Vaporizing Colds Rub

Menthol Ointment 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:
61734-030-03
Package Description:
50 g in 1 JAR
Product Code:
Proprietary Name:
Vaporizing Colds Rub
Non-Proprietary Name:
Menthol
Substance Name:
Camphor (synthetic); Eucalyptus Oil; Menthol
Usage Information:
See important warnings under "When using this product"adults and children 2 years and older:rub on the throat and chest in a thick layercover with a warm, dry cloth if desiredclothing should be loose about throat and chest to help vapors reach the nose and mouthuse up to three times daily or as directed by a doctorchildren under 2 years of age: ask a doctor
11-Digit NDC Billing Format:
61734003003
NDC to RxNorm Crosswalk:
  • RxCUI: 200293 - camphor 4.7 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Ointment
  • RxCUI: 200293 - camphor 0.047 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical Ointment
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Delon Laboratories (1990) Ltd
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >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.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-24-2011
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    61734-030-02113 g in 1 JAR

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 61734-030-03?

    The NDC Packaged Code 61734-030-03 is assigned to a package of 50 g in 1 jar of Vaporizing Colds Rub, a human over the counter drug labeled by Delon Laboratories (1990) Ltd. The product's dosage form is ointment and is administered via topical form.

    Is NDC 61734-030 included in the NDC Directory?

    Yes, Vaporizing Colds Rub with product code 61734-030 is active and included in the NDC Directory. The product was first marketed by Delon Laboratories (1990) Ltd on May 24, 2011 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 61734-030-03?

    The 11-digit format is 61734003003. 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
    5-3-261734-030-035-4-261734-0030-03