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  5. NDC Package Code: 67879-306-51 Sun Therape Pro Sport Spf-35

NDC Package 67879-306-51 Sun Therape Pro Sport Spf-35

Homosalate,Octinoxate,Oxybenzone,Octocrylene,Octisalate,Avobenzone Spray 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:
67879-306-51
Package Description:
1 BOTTLE, SPRAY in 1 BOX / 125 mL in 1 BOTTLE, SPRAY (67879-306-11)
Product Code:
67879-306
Proprietary Name:
Sun Therape Pro Sport Spf-35
Non-Proprietary Name:
Homosalate, Octinoxate, Oxybenzone, Octocrylene, Octisalate, Avobenzone
Substance Name:
Avobenzone; Homosalate; Octinoxate; Octisalate; Octocrylene; Oxybenzone
Usage Information:
• Apply liberally and evenly 15 minutes before sun exposure• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including:• Limit time in the sun, especially from 10 a.m.- 2 p.m.• Wear long-sleeve shirts, pants, hats, and sunglasses• Reapply at least every 2 hours• Use a water resistant sunscreen if swimming or sweating• Children under 6 months: Ask a doctor
11-Digit NDC Billing Format:
67879030651
Product Type:
Human Otc Drug
Labeler Name:
Pharmagel International 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.
    • Active Ingredient(s):
  • AVOBENZONE 3 g/100mL
  • HOMOSALATE 15 g/100mL
  • OCTINOXATE 7.5 g/100mL
  • OCTISALATE 5 g/100mL
  • OCTOCRYLENE 5.5 g/100mL
  • OXYBENZONE 6 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-10-2016
    Listing Expiration Date:
    12-31-2025
    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 67879-306-51?

    The NDC Packaged Code 67879-306-51 is assigned to a package of 1 bottle, spray in 1 box / 125 ml in 1 bottle, spray (67879-306-11) of Sun Therape Pro Sport Spf-35, a human over the counter drug labeled by Pharmagel International Inc. The product's dosage form is spray and is administered via topical form.

    Is NDC 67879-306 included in the NDC Directory?

    Yes, Sun Therape Pro Sport Spf-35 with product code 67879-306 is active and included in the NDC Directory. The product was first marketed by Pharmagel International Inc on June 10, 2016 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67879-306-51?

    The 11-digit format is 67879030651. 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
    5-3-267879-306-515-4-267879-0306-51