NDC Package 10742-8902-1 Red Cross Oral Pain Relief

Benzocaine Liquid 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:
10742-8902-1
Package Description:
1 BOTTLE in 1 BLISTER PACK / 3.7 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Red Cross Oral Pain Relief
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
•using tweezers, immerse cotton pellet in medication•apply pellet to affected area, then remove•adults and children 2 years and over: use up to 4 times daily or as directed by a dentist or doctor•children under 12 years: supervise while using this product•children under 2 years: ask a dentist or doctor
11-Digit NDC Billing Format:
10742890201
NDC to RxNorm Crosswalk:
  • RxCUI: 308657 - benzocaine 20 % Mucous Membrane Topical Solution
  • RxCUI: 308657 - benzocaine 200 MG/ML Mucous Membrane Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    The Mentholatum Company
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    06-01-2013
    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 10742-8902-1?

    The NDC Packaged Code 10742-8902-1 is assigned to a package of 1 bottle in 1 blister pack / 3.7 ml in 1 bottle of Red Cross Oral Pain Relief, a human over the counter drug labeled by The Mentholatum Company. The product's dosage form is liquid and is administered via topical form.

    Is NDC 10742-8902 included in the NDC Directory?

    Yes, Red Cross Oral Pain Relief with product code 10742-8902 is active and included in the NDC Directory. The product was first marketed by The Mentholatum Company on June 01, 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 10742-8902-1?

    The 11-digit format is 10742890201. 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
    5-4-110742-8902-15-4-210742-8902-01