NDC Package 35192-044-01 Mineral Sunscreen

Zinc Oxide Emulsion 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:
35192-044-01
Package Description:
61 g in 1 TUBE
Product Code:
Proprietary Name:
Mineral Sunscreen
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:
35192004401
Product Type:
Human Otc Drug
Labeler Name:
Ca-botana International
Dosage Form:
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
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):
    Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-15-2021
    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 35192-044-01?

    The NDC Packaged Code 35192-044-01 is assigned to a package of 61 g in 1 tube of Mineral Sunscreen, a human over the counter drug labeled by Ca-botana International. The product's dosage form is emulsion and is administered via topical form.

    Is NDC 35192-044 included in the NDC Directory?

    Yes, Mineral Sunscreen with product code 35192-044 is active and included in the NDC Directory. The product was first marketed by Ca-botana International on August 15, 2021 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 35192-044-01?

    The 11-digit format is 35192004401. 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
    5-3-235192-044-015-4-235192-0044-01