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  5. NDC Package Code: 70116-014-01 Eezysun Spf 50

NDC Package 70116-014-01 Eezysun Spf 50

Titanium Dioxide,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:
70116-014-01
Package Description:
70 TUBE in 1 CARTON / 100 mL in 1 TUBE
Product Code:
70116-014
Proprietary Name:
Eezysun Spf 50
Non-Proprietary Name:
Titanium Dioxide, Zinc Oxide
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
This product is used as Sunscreen. Helps prevent sunburn and protects against insects If used as directed with other sun protection measures ( See Directions) decreases the risk of skin cancer
11-Digit NDC Billing Format:
70116001401
Product Type:
Human Otc Drug
Labeler Name:
Bio Earth Manufacturing (pty) Ltd
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):
  • TITANIUM DIOXIDE 8 g/100mL
  • ZINC OXIDE 10 g/100mL
    • Pharmacologic Class(es):
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
    • 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:
    06-30-2023
    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 70116-014-01?

    The NDC Packaged Code 70116-014-01 is assigned to a package of 70 tube in 1 carton / 100 ml in 1 tube of Eezysun Spf 50, a human over the counter drug labeled by Bio Earth Manufacturing (pty) Ltd. The product's dosage form is cream and is administered via topical form.

    Is NDC 70116-014 included in the NDC Directory?

    Yes, Eezysun Spf 50 with product code 70116-014 is active and included in the NDC Directory. The product was first marketed by Bio Earth Manufacturing (pty) Ltd on June 30, 2023 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 70116-014-01?

    The 11-digit format is 70116001401. 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
    5-3-270116-014-015-4-270116-0014-01