NDC Package 37808-013-02 Athletes Foot Ultra

Butenafine Hydrochloride Cream 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:
37808-013-02
Package Description:
1 TUBE in 1 CARTON / 12 g in 1 TUBE
Product Code:
Proprietary Name:
Athletes Foot Ultra
Non-Proprietary Name:
Butenafine Hydrochloride
Substance Name:
Butenafine Hydrochloride
Usage Information:
Adults and children 12 years and older: use the tip of the cap to break the seal and open the tubewash the affected skin with soap and water and dry completely before applyingfor athlete's foot between the toes: apply to affected skin between and around the toes twice a day for 1 week (morning and night), or once a day for 4 weeks, or as directed by a doctor. Wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.Apply between and around the toes1 week twice a day or 4 weeks once a dayfor jock itch and ringworm: apply once a day to affected skin for 2 weeks or as directed by a doctor.wash hands after each usechildren under 12 years: ask a doctor
11-Digit NDC Billing Format:
37808001302
NDC to RxNorm Crosswalk:
  • RxCUI: 1298448 - butenafine HCl 1 % Topical Cream
  • RxCUI: 1298448 - butenafine hydrochloride 10 MG/ML Topical Cream
  • Product Type:
    Human Otc Drug
    Labeler Name:
    H E B
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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:
    ANDA205181
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-17-2017
    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 37808-013-02?

    The NDC Packaged Code 37808-013-02 is assigned to a package of 1 tube in 1 carton / 12 g in 1 tube of Athletes Foot Ultra, a human over the counter drug labeled by H E B. The product's dosage form is cream and is administered via topical form.

    Is NDC 37808-013 included in the NDC Directory?

    Yes, Athletes Foot Ultra with product code 37808-013 is active and included in the NDC Directory. The product was first marketed by H E B on November 17, 2017 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 37808-013-02?

    The 11-digit format is 37808001302. 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
    5-3-237808-013-025-4-237808-0013-02