Dr.jart Every Sun Day Sun Fluid Liquid
NDC Package 49404-154-01

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

Package Information

Dr.jart Every Sun Day Sun Fluid (homosalate, octinoxate, octisalate, octocrylene, avobenzone) liquids is ■ Apply liberally 15 minutes before sun exposure ■ Reapply at least every two hours ■ Use a water resistant sunscreen if swimming or sweating ■ Sun Protection Measures. This formulation utilizes a liquid delivery system. Marketed by Have & Be Co., Ltd., this product is identified by NDC 49404-154 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
49404-154-01
Package Description
1 CONTAINER in 1 CARTON / 100 mL in 1 CONTAINER
Product Code
49404-154
11-Digit Billing Format
49404015401

Clinical Specifications

Proprietary Name
Dr.jart Every Sun Day Sun Fluid
Non-Proprietary Name
Homosalate, Octinoxate, Octisalate, Octocrylene, Avobenzone
Substance Name
Avobenzone; Homosalate; Octinoxate; Octisalate; Octocrylene
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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 ■ Reapply at least every two 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 am to 2 pm * wear long-sleeved shirts, pants, hats, and sunglasses ■ Children under 6 months of age: ask a doctor

Regulatory & Marketing

Labeler Name
Have & Be Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-22-2022
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 49404-154-01 identifies a specific commercial package of 1 container in 1 carton / 100 ml in 1 container of Dr.jart Every Sun Day Sun Fluid, a human over the counter drug labeled by Have & Be Co., Ltd.. This liquid is formulated for topical use and contains avobenzone; homosalate; octinoxate; 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 Have & Be Co., Ltd. on December 22, 2022. The current certification is valid through December 31, 2026.

How is this Have & Be Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49404015401. 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)
49404-154-01
11-Digit CMS (5-4-2)
49404-0154-01

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