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  5. NDC Package Code: 61296-018-00 Biosolis Face Sunscreen Broad Spectrum Spf30

NDC Package 61296-018-00 Biosolis Face Sunscreen Broad Spectrum Spf30

Zinc Oxide 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:
61296-018-00
Package Description:
1 BOTTLE, PUMP in 1 BOX / 50 mL in 1 BOTTLE, PUMP
Product Code:
61296-018
Proprietary Name:
Biosolis Face Sunscreen Broad Spectrum Spf30
Non-Proprietary Name:
Zinc Oxide
Substance Name:
Zinc Oxide
Usage Information:
This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.
11-Digit NDC Billing Format:
61296001800
Product Type:
Human Otc Drug
Labeler Name:
Pro Vera Sa
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):
  • ZINC OXIDE 188 mg/mL
    • Pharmacologic Class(es):
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-07-2022
    End Marketing 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 61296-018-00?

    The NDC Packaged Code 61296-018-00 is assigned to a package of 1 bottle, pump in 1 box / 50 ml in 1 bottle, pump of Biosolis Face Sunscreen Broad Spectrum Spf30, a human over the counter drug labeled by Pro Vera Sa. The product's dosage form is cream and is administered via topical form.

    Is NDC 61296-018 included in the NDC Directory?

    Yes, Biosolis Face Sunscreen Broad Spectrum Spf30 with product code 61296-018 is active and included in the NDC Directory. The product was first marketed by Pro Vera Sa on January 07, 2022.

    What is the 11-digit format for NDC 61296-018-00?

    The 11-digit format is 61296001800. 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
    5-3-261296-018-005-4-261296-0018-00