Byt Bangytong Folliculitis Cream
NDC Package 87382-026-01

11-digit billing NDC: 87382002601
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Byt Bangytong Folliculitis (5% benzoyl peroxide folliculitis) cream is clean the skin thoroughly before applying. This formulation utilizes a cream delivery system. Marketed by Shenzhen Jindali Technology Co., Ltd, this product is identified by NDC 87382-026 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
87382-026-01
Package Description
100 g in 1 BOTTLE
Product Code
87382-026
11-Digit Billing Format
87382002601
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Byt Bangytong Folliculitis
Non-Proprietary Name
5% Benzoyl Peroxide Folliculitis
Substance Name
Benzoyl Peroxide
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
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)
BENZOYL PEROXIDE 5 g/100g
Usage Information
Clean the skin thoroughly before applying. Apply a thin layer to affected areas 1 to 3 times daily. Start with once daily, gradually increase to 2-3 times if needed. If dryness or peeling occurs, reduce to once daily or every other day.

Regulatory & Marketing

Labeler Name
Shenzhen Jindali Technology Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-18-2026
Listing Expiration
12-31-2027
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 87382-026-01 identifies a specific commercial package of 100 g in 1 bottle of Byt Bangytong Folliculitis, a human over the counter drug labeled by Shenzhen Jindali Technology Co., Ltd. This cream is formulated for topical use and contains benzoyl peroxide 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 Shenzhen Jindali Technology Co., Ltd on August 18, 2026. The current certification is valid through December 31, 2027.

How is this Shenzhen Jindali Technology Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87382002601. 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)
87382-026-01
11-Digit CMS (5-4-2)
87382-0026-01

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