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  5. NDC Package Code: 72296-050-50 Tula Skincare Protect Glow Daily Sunscreen Gel Broad Spectrum Spf 30

NDC Package 72296-050-50 Tula Skincare Protect Glow Daily Sunscreen Gel Broad Spectrum Spf 30

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:
72296-050-50
Package Description:
1 TUBE in 1 CARTON / 50 g in 1 TUBE
Product Code:
72296-050
Proprietary Name:
Tula Skincare Protect Glow Daily Sunscreen Gel Broad Spectrum Spf 30
Non-Proprietary Name:
Tula Skincare Protect Glow Daily Sunscreen Gel Broad Spectrum Spf 30
Substance Name:
Avobenzone; Homosalate; Octisalate
Usage Information:
• apply generously 15 minutes before sun exposure • reapply at least every 2 hours • use a water-resistant sunscreen if swimming or sweating • 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 • children under 6 months of age: Ask a doctor
11-Digit NDC Billing Format:
72296005050
Product Type:
Human Otc Drug
Labeler Name:
Tula Life Llc
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 3 g/100g
  • HOMOSALATE 10 g/100g
  • OCTISALATE 5 g/100g
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-22-2024
    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 72296-050-50?

    The NDC Packaged Code 72296-050-50 is assigned to a package of 1 tube in 1 carton / 50 g in 1 tube of Tula Skincare Protect Glow Daily Sunscreen Gel Broad Spectrum Spf 30, a human over the counter drug labeled by Tula Life Llc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 72296-050 included in the NDC Directory?

    Yes, Tula Skincare Protect Glow Daily Sunscreen Gel Broad Spectrum Spf 30 with product code 72296-050 is active and included in the NDC Directory. The product was first marketed by Tula Life Llc on March 22, 2024 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 72296-050-50?

    The 11-digit format is 72296005050. 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
    5-3-272296-050-505-4-272296-0050-50