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  5. NDC Package Code: 66820-0400-1 Sekkisei Herbal Uv Defense Gel

NDC Package 66820-0400-1 Sekkisei Herbal Uv Defense Gel

Avobenzone,Homosalate,Octisalate,And Octocrylene Gel 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:
66820-0400-1
Package Description:
1 TUBE in 1 CARTON / 30 mL in 1 TUBE
Product Code:
66820-0400
Proprietary Name:
Sekkisei Herbal Uv Defense Gel
Non-Proprietary Name:
Avobenzone, Homosalate, Octisalate, And Octocrylene
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene
Usage Information:
For sunscreen use: • apply liberally 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: Ask a doctor
11-Digit NDC Billing Format:
66820040001
Product Type:
Human Otc Drug
Labeler Name:
Kose America, Inc.
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-03-2024
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 66820-0400-1?

The NDC Packaged Code 66820-0400-1 is assigned to a package of 1 tube in 1 carton / 30 ml in 1 tube of Sekkisei Herbal Uv Defense Gel, a human over the counter drug labeled by Kose America, Inc.. The product's dosage form is gel and is administered via topical form.

Is NDC 66820-0400 included in the NDC Directory?

Yes, Sekkisei Herbal Uv Defense Gel with product code 66820-0400 is active and included in the NDC Directory. The product was first marketed by Kose America, Inc. on January 03, 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 66820-0400-1?

The 11-digit format is 66820040001. 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 5-4-1 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
5-4-166820-0400-15-4-266820-0400-01