NDC Package 10210-0027-1 Carmex Cold Sore Treatment External Analgesic Skin Protectant

Benzocaine,White Petrolatum Cream 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:
10210-0027-1
Package Description:
1 TUBE in 1 BLISTER PACK / 2 g in 1 TUBE
Product Code:
Proprietary Name:
Carmex Cold Sore Treatment External Analgesic Skin Protectant
Non-Proprietary Name:
Benzocaine, White Petrolatum
Substance Name:
Benzocaine; White Petrolatum
Usage Information:
Adults and children 2 years of age and olderApply to affected area (lips) not more than 3 to 4 times daily Children 2-12 years of ageShould be supervised in use of this productChildren under 2 years of age Ask a doctor
11-Digit NDC Billing Format:
10210002701
NDC to RxNorm Crosswalk:
  • RxCUI: 2477289 - benzocaine 10 % / petrolatum 45.9 % Topical Cream
  • RxCUI: 2477289 - benzocaine 100 MG/ML / petrolatum 459 MG/ML Topical Cream
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Carma Laboratories, Inc.
    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.
  • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-02-2017
    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 10210-0027-1?

    The NDC Packaged Code 10210-0027-1 is assigned to a package of 1 tube in 1 blister pack / 2 g in 1 tube of Carmex Cold Sore Treatment External Analgesic Skin Protectant, a human over the counter drug labeled by Carma Laboratories, Inc.. The product's dosage form is cream and is administered via topical form.

    Is NDC 10210-0027 included in the NDC Directory?

    Yes, Carmex Cold Sore Treatment External Analgesic Skin Protectant with product code 10210-0027 is active and included in the NDC Directory. The product was first marketed by Carma Laboratories, Inc. on March 02, 2017 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 10210-0027-1?

    The 11-digit format is 10210002701. 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
    5-4-110210-0027-15-4-210210-0027-01