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  5. NDC Package Code: 87243-123-35 Sunscreen

NDC Package 87243-123-35 Sunscreen

Japanese Sunscreen Spf 50 Super Water Gel Sunscreen 4.22floz(125g) Refill Cream Cutaneous - 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:
87243-123-35
Package Description:
5 CANISTER in 1 BOX / 1 CREAM in 1 CANISTER
Product Code:
87243-123
Proprietary Name:
Sunscreen
Non-Proprietary Name:
Japanese Sunscreen Spf 50 Super Water Gel Sunscreen 4.22floz(125g) Refill
Substance Name:
Octinoxate
Usage Information:
helps prevent sunburn apply liberally 15 minutes before sun exposure after 80 minutes of swimming or sweating immediately after towel drying
11-Digit NDC Billing Format:
87243012335
Product Type:
Human Otc Drug
Labeler Name:
Maidora Co.,ltd
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Cutaneous - Administration to the skin.
Active Ingredient(s):
OCTINOXATE 1 g/1
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
11-21-2025
Listing Expiration Date:
12-31-2026
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 87243-123-35?

The NDC Packaged Code 87243-123-35 is assigned to a package of 5 canister in 1 box / 1 cream in 1 canister of Sunscreen, a human over the counter drug labeled by Maidora Co.,ltd. The product's dosage form is cream and is administered via cutaneous form.

Is NDC 87243-123 included in the NDC Directory?

Yes, Sunscreen with product code 87243-123 is active and included in the NDC Directory. The product was first marketed by Maidora Co.,ltd on November 21, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 87243-123-35?

The 11-digit format is 87243012335. 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
5-3-287243-123-355-4-287243-0123-35