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  5. NDC Package Code: 30142-879-13 Daily Spf 15

NDC Package 30142-879-13 Daily Spf 15

Avobenzone,Octinoxate,Octisalate 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:
30142-879-13
Package Description:
120 mL in 1 TUBE
Product Code:
30142-879
Proprietary Name:
Daily Spf 15
Non-Proprietary Name:
Avobenzone, Octinoxate, Octisalate
Substance Name:
Avobenzone; Octinoxate; Octisalate
Usage Information:
Useshelps prevent sunburnif used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
11-Digit NDC Billing Format:
30142087913
Product Type:
Human Otc Drug
Labeler Name:
The Kroger Co
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):
  • AVOBENZONE 30 mg/mL
  • OCTINOXATE 75 mg/mL
  • OCTISALATE 20 mg/mL
    • 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:
    06-07-2018
    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 30142-879-13?

    The NDC Packaged Code 30142-879-13 is assigned to a package of 120 ml in 1 tube of Daily Spf 15, a human over the counter drug labeled by The Kroger Co. The product's dosage form is lotion and is administered via topical form.

    Is NDC 30142-879 included in the NDC Directory?

    Yes, Daily Spf 15 with product code 30142-879 is active and included in the NDC Directory. The product was first marketed by The Kroger Co on June 07, 2018 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 30142-879-13?

    The 11-digit format is 30142087913. 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
    5-3-230142-879-135-4-230142-0879-13