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  5. NDC Package Code: 0096-0687-04 Solbar Avo Spf35

NDC Package 0096-0687-04 Solbar Avo Spf35

Cream 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:
0096-0687-04
Package Description:
119 g in 1 BOTTLE
Product Code:
0096-0687
Proprietary Name:
Solbar Avo Spf35
Non-Proprietary Name:
Solbar Avo Spf35
Substance Name:
Avobenzone; Homosalate; Octinoxate; Oxybenzone
Usage Information:
Helps prevent sunburn. If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun. Dosage and Administration: Apply liberally and evenly to all sun exposed areas of DRY skin 15 minutes before sun exposure. Reapply after 80 minutes of swimming or sweating and immediately after towel drying. Apply at least every 2 hours. For children under 6 months, ask a physician.
11-Digit NDC Billing Format:
00096068704
Product Type:
Human Otc Drug
Labeler Name:
Person And Covey
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):
  • AVOBENZONE .03 g/g
  • HOMOSALATE .08 g/g
  • OCTINOXATE .075 g/g
  • OXYBENZONE .06 g/g
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-01-1996
    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 0096-0687-04?

    The NDC Packaged Code 0096-0687-04 is assigned to a package of 119 g in 1 bottle of Solbar Avo Spf35, a human over the counter drug labeled by Person And Covey. The product's dosage form is cream and is administered via topical form.

    Is NDC 0096-0687 included in the NDC Directory?

    Yes, Solbar Avo Spf35 with product code 0096-0687 is active and included in the NDC Directory. The product was first marketed by Person And Covey on June 01, 1996 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 0096-0687-04?

    The 11-digit format is 00096068704. 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
    4-4-20096-0687-045-4-200096-0687-04