NDC Package 80069-007-01 Vasocaine

Lidocaine Hcl,Epinephrine Hcl Spray 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:
80069-007-01
Package Description:
118.294 mL in 1 BOTTLE, PUMP
Product Code:
Proprietary Name:
Vasocaine
Non-Proprietary Name:
Lidocaine Hcl, Epinephrine Hcl
Substance Name:
Epinephrine Hydrochloride; Lidocaine Hydrochloride
Usage Information:
Uses: External Use Only.  Temporarily relieves pain, itching or swelling associated with anorectal disorders or pain sensitive procedures.
11-Digit NDC Billing Format:
80069000701
NDC to RxNorm Crosswalk:
  • RxCUI: 2462017 - EPINEPHrine HCl 0.01 % / lidocaine HCl 5 % Topical Spray
  • RxCUI: 2462017 - epinephrine hydrochloride 0.1 MG/ML / lidocaine hydrochloride 50 MG/ML Topical Spray
  • RxCUI: 2462017 - epinephrine hydrochloride 0.01 % / lidocaine hydrochloride 5 % Topical Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Dermal Source, Inc.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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:
    M015
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-01-2005
    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 80069-007-01?

    The NDC Packaged Code 80069-007-01 is assigned to a package of 118.294 ml in 1 bottle, pump of Vasocaine, a human over the counter drug labeled by Dermal Source, Inc.. The product's dosage form is spray and is administered via topical form.

    Is NDC 80069-007 included in the NDC Directory?

    Yes, Vasocaine with product code 80069-007 is active and included in the NDC Directory. The product was first marketed by Dermal Source, Inc. on June 01, 2005 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 80069-007-01?

    The 11-digit format is 80069000701. 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
    5-3-280069-007-015-4-280069-0007-01