NDC Package 66902-235-03 Fast Freeze Lidocaine Roll-on

Lidocaine Hydrochloride,Benzyl Alcohol 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:
66902-235-03
Package Description:
89 mL in 1 CONTAINER
Product Code:
Proprietary Name:
Fast Freeze Lidocaine Roll-on
Non-Proprietary Name:
Lidocaine Hydrochloride, Benzyl Alcohol
Substance Name:
Benzyl Alcohol; Lidocaine Hydrochloride
Usage Information:
Adults and children 12 years of age and over clean and dry affected area apply to affected area not more than 3 to 4 times daily children 12 years or younger ask a doctor
11-Digit NDC Billing Format:
66902023503
NDC to RxNorm Crosswalk:
  • RxCUI: 1943537 - benzyl alcohol 10 % / lidocaine HCl 4 % Topical Solution
  • RxCUI: 1943537 - benzyl alcohol 0.1 ML/ML / lidocaine hydrochloride 40 MG/ML Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Natural Essentials, Inc.
    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.
  • Sample Package:
    No
    FDA Application Number:
    part348
    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:
    07-10-2020
    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 66902-235-03?

    The NDC Packaged Code 66902-235-03 is assigned to a package of 89 ml in 1 container of Fast Freeze Lidocaine Roll-on, a human over the counter drug labeled by Natural Essentials, Inc.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 66902-235 included in the NDC Directory?

    Yes, Fast Freeze Lidocaine Roll-on with product code 66902-235 is active and included in the NDC Directory. The product was first marketed by Natural Essentials, Inc. on July 10, 2020 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 66902-235-03?

    The 11-digit format is 66902023503. 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
    5-3-266902-235-035-4-266902-0235-03