Beet The Sun Lightweight Sunscreen Broad Spectrum Spf 40 Pa Lotion
NDC Package 83493-150-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Beet The Sun Lightweight Sunscreen Broad Spectrum Spf 40 Pa (avobenzone, homosalate, octisalate, octocrylene) lotions is apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating Reapply at least every 2 hoursSun Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. This formulation utilizes a lotion delivery system. Marketed by Krave Beauty, Llc, this product is identified by NDC 83493-150 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
83493-150-01
Package Description
50 mL in 1 TUBE
Product Code
83493-150
11-Digit Billing Format
83493015001

Clinical Specifications

Proprietary Name
Beet The Sun Lightweight Sunscreen Broad Spectrum Spf 40 Pa
Non-Proprietary Name
Avobenzone, Homosalate, Octisalate, Octocrylene
Substance Name
Avobenzone; Homosalate; Octisalate; Octocrylene
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
Administration Route
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)
Usage Information
Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating Reapply at least every 2 hoursSun Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen 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: Ask a doctor

Regulatory & Marketing

Labeler Name
Krave Beauty, Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-01-2023
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 83493-150-01 identifies a specific commercial package of 50 ml in 1 tube of Beet The Sun Lightweight Sunscreen Broad Spectrum Spf 40 Pa, a human over the counter drug labeled by Krave Beauty, Llc. This lotion is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Krave Beauty, Llc on March 01, 2023. The current certification is valid through December 31, 2026.

How is this Krave Beauty, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83493015001. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
83493-150-01
11-Digit CMS (5-4-2)
83493-0150-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.