NDC Package 60630-077-04 Dentek Instant Pain Relief Maximum Strength

Benzocaine Liquid Dental; 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:
60630-077-04
Package Description:
1 VIAL, GLASS in 1 CARTON / 3.5 mL in 1 VIAL, GLASS (60630-077-03)
Product Code:
Proprietary Name:
Dentek Instant Pain Relief Maximum Strength
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Use for the temporary relief of pain due to: . toothaches . canker sore . cold sores . sore gums
11-Digit NDC Billing Format:
60630007704
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:
    Dentek Oral Care, 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):
  • Dental - Administration to a tooth or teeth.
  • 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:
    07-31-2015
    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 60630-077-04?

    The NDC Packaged Code 60630-077-04 is assigned to a package of 1 vial, glass in 1 carton / 3.5 ml in 1 vial, glass (60630-077-03) of Dentek Instant Pain Relief Maximum Strength, a human over the counter drug labeled by Dentek Oral Care, Inc.. The product's dosage form is liquid and is administered via dental; topical form.

    Is NDC 60630-077 included in the NDC Directory?

    Yes, Dentek Instant Pain Relief Maximum Strength with product code 60630-077 is active and included in the NDC Directory. The product was first marketed by Dentek Oral Care, Inc. on July 31, 2015 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 60630-077-04?

    The 11-digit format is 60630007704. 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
    5-3-260630-077-045-4-260630-0077-04