NDC Package 81781-101-50 Daily Face Sunscreen Broad Spectrum Spf 30

Zinc Oxide Cream 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:
81781-101-50
Package Description:
1 TUBE in 1 CARTON / 48 g in 1 TUBE
Product Code:
Proprietary Name:
Daily Face Sunscreen Broad Spectrum Spf 30
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:
81781010150
Product Type:
Human Otc Drug
Labeler Name:
Lilyana Naturals Llc
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):
    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:
    07-15-2021
    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 81781-101-50?

    The NDC Packaged Code 81781-101-50 is assigned to a package of 1 tube in 1 carton / 48 g in 1 tube of Daily Face Sunscreen Broad Spectrum Spf 30, a human over the counter drug labeled by Lilyana Naturals Llc. The product's dosage form is cream and is administered via topical form.

    Is NDC 81781-101 included in the NDC Directory?

    Yes, Daily Face Sunscreen Broad Spectrum Spf 30 with product code 81781-101 is active and included in the NDC Directory. The product was first marketed by Lilyana Naturals Llc on July 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 81781-101-50?

    The 11-digit format is 81781010150. 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
    5-3-281781-101-505-4-281781-0101-50