NDC Package 60289-297-24 Lumior Daylight Moisturizer Broad Spectrum Spf 20

Avobenzone,Homosalate,Octisalate,And Octocrylene Lotion 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:
60289-297-24
Package Description:
1 JAR in 1 CARTON / 50 mL in 1 JAR
Product Code:
Proprietary Name:
Lumior Daylight Moisturizer Broad Spectrum Spf 20
Non-Proprietary Name:
Avobenzone, Homosalate, Octisalate, And Octocrylene
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene
Usage Information:
Apply every morning in gentle, upward strokes to a clean face and neck. Feel luminous, every dayapply daily for a clearer, brighter complexionchildren under 6 months of age: Ask a doctorSun 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including:limit time in the sun, especially from 10a.m.-2 p.m.wear long-sleeved shirts, pants, hats and sunglasses
11-Digit NDC Billing Format:
60289029724
Product Type:
Human Otc Drug
Labeler Name:
Ahava Dead Sea Laboratories Ltd
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.
  • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-01-2020
    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 60289-297-24?

    The NDC Packaged Code 60289-297-24 is assigned to a package of 1 jar in 1 carton / 50 ml in 1 jar of Lumior Daylight Moisturizer Broad Spectrum Spf 20, a human over the counter drug labeled by Ahava Dead Sea Laboratories Ltd. The product's dosage form is lotion and is administered via topical form.

    Is NDC 60289-297 included in the NDC Directory?

    Yes, Lumior Daylight Moisturizer Broad Spectrum Spf 20 with product code 60289-297 is active and included in the NDC Directory. The product was first marketed by Ahava Dead Sea Laboratories Ltd on October 01, 2020 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 60289-297-24?

    The 11-digit format is 60289029724. 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
    5-3-260289-297-245-4-260289-0297-24