NDC Package 76150-261-51 Habit Spf 41

Facial 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:
76150-261-51
Package Description:
30 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Habit Spf 41
Non-Proprietary Name:
Facial
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene
Usage Information:
Apply generously 15 minutes before sun exposureReapply at least every 2 hoursUse a warer-resistant sunscreen if swimming or sweatingReapply after swimming or sweatingChildren under 6 monts-age: Ask a doctorSun Protection Meaures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including:-limit time in the sun, especially from 10a.m. - 2 p.m.-wear long-sleeved shirts, pants, hats, and sunglasses.
11-Digit NDC Billing Format:
76150026151
Billing Unit:
C112160
Product Type:
Human Otc Drug
Labeler Name:
Bell International Laboratories, Inc
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:
    part352
    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:
    01-01-2020
    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 76150-261-51?

    The NDC Packaged Code 76150-261-51 is assigned to a package of 30 ml in 1 bottle, plastic of Habit Spf 41, a human over the counter drug labeled by Bell International Laboratories, Inc. The product's dosage form is spray and is administered via topical form.

    Is NDC 76150-261 included in the NDC Directory?

    Yes, Habit Spf 41 with product code 76150-261 is active and included in the NDC Directory. The product was first marketed by Bell International Laboratories, Inc on January 01, 2020 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 NDC billing unit for package 76150-261-51?

    The contents of this package are billed C112160

    What is the 11-digit format for NDC 76150-261-51?

    The 11-digit format is 76150026151. 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
    5-3-276150-261-515-4-276150-0261-51