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  5. NDC Package Code: 0187-5500-04 Purpose

NDC Package 0187-5500-04 Purpose

Octinoxate,Octisalate And Oxybenzone Lotion 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:
0187-5500-04
Package Description:
1 BOTTLE, PUMP in 1 CARTON / 118 mL in 1 BOTTLE, PUMP
Product Code:
0187-5500
Proprietary Name:
Purpose
Non-Proprietary Name:
Octinoxate, Octisalate And Oxybenzone
Substance Name:
Octinoxate; Octisalate; Oxybenzone
Usage Information:
■ apply generously and evenly 15 minutes before sun exposure■ apply to all skin exposed to the sun■ use a water resistant sunscreen if swimming or sweating■ reapply at least every 2 hours■ children under 6 months of age:    Ask a doctor
11-Digit NDC Billing Format:
00187550004
Product Type:
Human Otc Drug
Labeler Name:
Bausch Health Us Llc
Dosage Form:
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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):
  • OCTINOXATE 76 mg/mL
  • OCTISALATE 50 mg/mL
  • OXYBENZONE 30 mg/mL
    • 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:
    10-07-2013
    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 0187-5500-04?

    The NDC Packaged Code 0187-5500-04 is assigned to a package of 1 bottle, pump in 1 carton / 118 ml in 1 bottle, pump of Purpose, a human over the counter drug labeled by Bausch Health Us Llc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 0187-5500 included in the NDC Directory?

    Yes, Purpose with product code 0187-5500 is active and included in the NDC Directory. The product was first marketed by Bausch Health Us Llc on October 07, 2013 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 0187-5500-04?

    The 11-digit format is 00187550004. 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
    4-4-20187-5500-045-4-200187-5500-04