NDC Package 0363-7731-30 Undecylenic Acid

Anti-fungal Liquid Liquid 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:
0363-7731-30
Package Description:
30 g in 1 BOTTLE, WITH APPLICATOR
Product Code:
Proprietary Name:
Undecylenic Acid
Non-Proprietary Name:
Anti-fungal Liquid
Substance Name:
Undecylenic Acid
Usage Information:
Read all warnings and directions. Use only as directed.clean the affected area and dry thoroughlyapply a thin layer of the product over the affecter area twice daily (morning and night) or as directed by a doctorsupervise children in the use of this productfor athlete's foot: pay special attention to spaces between toeswear well-fitting, ventilated shoes, and change shoes and socks at least once dailyfor athlete's foot and ringworm, use daily for 4 weeks. If conditions persists longer, consult a doctorthis product is not effective on the scalp or nails
11-Digit NDC Billing Format:
00363773130
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 998329 - undecylenic acid 25 % Topical Solution
  • RxCUI: 998329 - undecylenic acid 250 MG/ML Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Walgreen Company
    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):
    Sample Package:
    No
    FDA Application Number:
    M005
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-16-2012
    End Marketing Date:
    05-31-2024
    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 0363-7731-30?

    The NDC Packaged Code 0363-7731-30 is assigned to a package of 30 g in 1 bottle, with applicator of Undecylenic Acid, a human over the counter drug labeled by Walgreen Company. The product's dosage form is liquid and is administered via topical form.

    Is NDC 0363-7731 included in the NDC Directory?

    Yes, Undecylenic Acid with product code 0363-7731 is active and included in the NDC Directory. The product was first marketed by Walgreen Company on August 16, 2012.

    What is the NDC billing unit for package 0363-7731-30?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0363-7731-30?

    The 11-digit format is 00363773130. 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 4-4-2 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
    4-4-20363-7731-305-4-200363-7731-30