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  5. NDC Package Code: 65121-209-32 Biochemistry Pain Relief Foot Active

NDC Package 65121-209-32 Biochemistry Pain Relief Foot Active

Benzyl Alcohol,Lidocaine Hydrochloride Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
65121-209-32
Package Description:
1 BOTTLE, SPRAY in 1 CARTON / 60 mL in 1 BOTTLE, SPRAY
Product Code:
65121-209
Proprietary Name:
Biochemistry Pain Relief Foot Active
Non-Proprietary Name:
Benzyl Alcohol, Lidocaine Hydrochloride
Substance Name:
Benzyl Alcohol; Lidocaine Hydrochloride
Usage Information:
Over 12-yearsApply directly to affected areaDo not wrap affected areaDo not use more than four times per day
11-Digit NDC Billing Format:
65121020932
NDC to RxNorm Crosswalk:
  • RxCUI: 1488328 - benzyl alcohol 19 % / lidocaine HCl 4 % Topical Spray
  • RxCUI: 1488328 - benzyl alcohol 0.19 ML/ML / lidocaine hydrochloride 40 MG/ML Topical Spray
  • RxCUI: 1488328 - benzyl alcohol 19 % / lidocaine hydrochloride 4 % Topical Spray
  • RxCUI: 1488333 - biochemistry Heel No Pain 19 % / 4 % Topical Spray
  • RxCUI: 1488333 - benzyl alcohol 0.19 ML/ML / lidocaine hydrochloride 40 MG/ML Topical Spray [Biochemistry Heel No Pain]
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Pure Source, Llc
    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):
  • BENZYL ALCOHOL 190 mg/mL
  • LIDOCAINE HYDROCHLORIDE 40 mg/mL
    • Pharmacologic Class(es):
  • Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
  • Amides - [CS]
  • Antiarrhythmic - [EPC] (Established Pharmacologic Class)
  • Local Anesthesia - [PE] (Physiologic Effect)
  • Pediculicide - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-06-2014
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    65121-209-311 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 65121-209-32?

    The NDC Packaged Code 65121-209-32 is assigned to a package of 1 bottle, spray in 1 carton / 60 ml in 1 bottle, spray of Biochemistry Pain Relief Foot Active, a human over the counter drug labeled by Pure Source, Llc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 65121-209 included in the NDC Directory?

    Yes, Biochemistry Pain Relief Foot Active with product code 65121-209 is active and included in the NDC Directory. The product was first marketed by Pure Source, Llc on February 06, 2014 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 65121-209-32?

    The 11-digit format is 65121020932. 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
    5-3-265121-209-325-4-265121-0209-32