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  5. NDC Package Code: 59735-188-01 Your Name Tinted Primer Broad Spectrum Spf 20- Deep

NDC Package 59735-188-01 Your Name Tinted Primer Broad Spectrum Spf 20- Deep

Your Name Tinted Primer 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:
59735-188-01
Package Description:
1 BOTTLE in 1 CARTON / 36 mL in 1 BOTTLE
Product Code:
59735-188
Proprietary Name:
Your Name Tinted Primer Broad Spectrum Spf 20- Deep
Non-Proprietary Name:
Your Name Tinted Primer
Substance Name:
Octinoxate; Titanium Dioxide
Usage Information:
Stop use and ask a doctor if rash occurs.
11-Digit NDC Billing Format:
59735018801
Product Type:
Human Otc Drug
Labeler Name:
Mana Products, Inc.
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):
  • OCTINOXATE 7.5 g/36mL
  • TITANIUM DIOXIDE 5 g/36mL
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-01-2011
    Listing Expiration Date:
    12-31-2025
    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 59735-188-01?

    The NDC Packaged Code 59735-188-01 is assigned to a package of 1 bottle in 1 carton / 36 ml in 1 bottle of Your Name Tinted Primer Broad Spectrum Spf 20- Deep, a human over the counter drug labeled by Mana Products, Inc.. The product's dosage form is cream and is administered via topical form.

    Is NDC 59735-188 included in the NDC Directory?

    Yes, Your Name Tinted Primer Broad Spectrum Spf 20- Deep with product code 59735-188 is active and included in the NDC Directory. The product was first marketed by Mana Products, Inc. on February 01, 2011 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 59735-188-01?

    The 11-digit format is 59735018801. 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
    5-3-259735-188-015-4-259735-0188-01