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  5. NDC Package Code: 16864-690-01 Dermoplast Pain Relieving

NDC Package 16864-690-01 Dermoplast Pain Relieving

Benzocaine,Menthol Spray Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
16864-690-01
Package Description:
78 g in 1 CAN
Product Code:
16864-690
Proprietary Name:
Dermoplast Pain Relieving
Non-Proprietary Name:
Benzocaine, Menthol
Substance Name:
Benzocaine; Menthol
Usage Information:
 Adults and children 2 years of age and older apply to affected area not more than 3 to 4 times daily Children under 2 years of age  consult a doctor  to use this product, hold the can 6 to 12 inches away from the affected area. Direct spray nozzle towards skin and press button to activate spray.to apply to face, spray in palm of hand and gently apply
11-Digit NDC Billing Format:
16864069001
NDC to RxNorm Crosswalk:
  • RxCUI: 199864 - benzocaine 20 % / menthol 0.5 % Topical Spray
  • RxCUI: 199864 - benzocaine 200 MG/ML / menthol 5 MG/ML Topical Spray
  • RxCUI: 763484 - Dermoplast 20 % / 0.5 % Topical Spray
  • RxCUI: 763484 - benzocaine 200 MG/ML / menthol 5 MG/ML Topical Spray [Dermoplast Pain]
  • RxCUI: 763484 - Dermoplast Insect Itch and Sting Relief (benzocaine 20 % / menthol 0.5 % ) Topical Spray
Product Type:
Human Otc Drug
Labeler Name:
Advantice Health
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.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
03-18-2022
Listing Expiration Date:
12-31-2025
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 16864-690-01?

The NDC Packaged Code 16864-690-01 is assigned to a package of 78 g in 1 can of Dermoplast Pain Relieving, a human over the counter drug labeled by Advantice Health. The product's dosage form is spray and is administered via topical form.

Is NDC 16864-690 included in the NDC Directory?

Yes, Dermoplast Pain Relieving with product code 16864-690 is active and included in the NDC Directory. The product was first marketed by Advantice Health on March 18, 2022 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 16864-690-01?

The 11-digit format is 16864069001. 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
5-3-216864-690-015-4-216864-0690-01