NDC Package 52915-040-29 Spf30 Summer Blend Sunscreen

Titanium Dioxide Lotion/shampoo 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:
52915-040-29
Package Description:
82 g in 1 TUBE
Product Code:
Proprietary Name:
Spf30 Summer Blend Sunscreen
Non-Proprietary Name:
Titanium Dioxide
Substance Name:
Titanium Dioxide
Usage Information:
Apply liberally 30 minutes before sun exposureReapply – after 80 minutes of swimming or sweating immediately after towel drying – at least every 2 hoursChildren under 6 months: 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 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
11-Digit NDC Billing Format:
52915004029
Product Type:
Human Otc Drug
Labeler Name:
Organic & Sustainable Beauty
Dosage Form:
Lotion/shampoo - A lotion dosage form which has a soap or detergent that is usually used to clean the hair and scalp; it is often used as a vehicle for dermatologic agents.
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):
    Sample Package:
    No
    FDA Application Number:
    part352
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    04-01-2010
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

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    Frequently Asked Questions

    What is NDC 52915-040-29?

    The NDC Packaged Code 52915-040-29 is assigned to a package of 82 g in 1 tube of Spf30 Summer Blend Sunscreen, a human over the counter drug labeled by Organic & Sustainable Beauty. The product's dosage form is lotion/shampoo and is administered via topical form.

    Is NDC 52915-040 included in the NDC Directory?

    Yes, Spf30 Summer Blend Sunscreen with product code 52915-040 is active and included in the NDC Directory. The product was first marketed by Organic & Sustainable Beauty on April 01, 2010 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 52915-040-29?

    The 11-digit format is 52915004029. 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
    5-3-252915-040-295-4-252915-0040-29