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  5. NDC Package Code: 0316-0263-02 Panoxyl Oil Control Moisturizer

NDC Package 0316-0263-02 Panoxyl Oil Control Moisturizer

Titanium Dioxide And Zinc Oxide Lotion 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:
0316-0263-02
Package Description:
1 TUBE in 1 CARTON / 48 g in 1 TUBE
Product Code:
0316-0263
Proprietary Name:
Panoxyl Oil Control Moisturizer
Non-Proprietary Name:
Titanium Dioxide And Zinc Oxide
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
• Shake well prior to use• Apply liberally to dry skin 15 minutes before sun exposure• For topical use only• Keep out of reach of children • Children under 6 months: ask a doctor• 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 a Broad Spectrum SPF value 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-sleeved shirts, pants, hats, and sunglasses.• Reapply to dry skin: • At least every 2 hours • Use a water resistant suscreen if swimming for sweating
11-Digit NDC Billing Format:
00316026302
Product Type:
Human Otc Drug
Labeler Name:
Crown Laboratories
Dosage Form:
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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):
  • TITANIUM DIOXIDE 10 mg/g
  • ZINC OXIDE 83.4 mg/g
    • 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:
    03-09-2021
    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 0316-0263-02?

    The NDC Packaged Code 0316-0263-02 is assigned to a package of 1 tube in 1 carton / 48 g in 1 tube of Panoxyl Oil Control Moisturizer, a human over the counter drug labeled by Crown Laboratories. The product's dosage form is lotion and is administered via topical form.

    Is NDC 0316-0263 included in the NDC Directory?

    Yes, Panoxyl Oil Control Moisturizer with product code 0316-0263 is active and included in the NDC Directory. The product was first marketed by Crown Laboratories on March 09, 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 0316-0263-02?

    The 11-digit format is 00316026302. 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
    4-4-20316-0263-025-4-200316-0263-02