NDC Package 16864-682-01 Dermoplast Insect Itch And Sting Relief

Benzocaine And Levomenthol 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:
16864-682-01
Package Description:
78 g in 1 CAN
Product Code:
Proprietary Name:
Dermoplast Insect Itch And Sting Relief
Non-Proprietary Name:
Benzocaine And Levomenthol
Substance Name:
Benzocaine; Levomenthol
Usage Information:
Adults and children 2 years of age and olderapply to affected area not more than 3 to 4 times dailyChildren under 2 years of ageconsult a doctorto 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:
16864068201
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, Llc
    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:
    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:
    05-15-2021
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

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    Frequently Asked Questions

    What is NDC 16864-682-01?

    The NDC Packaged Code 16864-682-01 is assigned to a package of 78 g in 1 can of Dermoplast Insect Itch And Sting Relief, a human over the counter drug labeled by Advantice Health, Llc. The product's dosage form is spray and is administered via topical form.

    Is NDC 16864-682 included in the NDC Directory?

    Yes, Dermoplast Insect Itch And Sting Relief with product code 16864-682 is active and included in the NDC Directory. The product was first marketed by Advantice Health, Llc on May 15, 2021 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 16864-682-01?

    The 11-digit format is 16864068201. 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
    5-3-216864-682-015-4-216864-0682-01