Sulfur
NDC Package 78565-106-02

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Sulfur is make lather with sponge.Apply to affected areas.Leave lather on skin for 3 to 5 minutes.Rinse thoroughly with water and gently pat dry with a clean toweI.May be used 1 to 3 times a day or as directed by a doctor Make lather with sponge.Apply to affected areas.Leave lather on skin for 3 to 5 minutes.Rinse thoroughly with water and gently pat dry with a clean toweI.May be used 1 to 3 times a day or as directed by a doctor. Marketed by Meixin Beauty & Health Care Products Co., Ltd., this product is identified by NDC 78565-106 and is authorized under FDA application part358H.

Identification & Billing

NDC Package Code
78565-106-02
Package Description
240 g in 1 BOX
Product Code
78565-106
11-Digit Billing Format
78565010602
RxNorm Crosswalk
  • RxCUI: 2586352 - salicylic acid 3 % / sulfur 10 % Medicated Liquid Soap
  • RxCUI: 2586352 - salicylic acid 30 MG/ML / sulfur 100 MG/ML Medicated Liquid Soap

Clinical Specifications

Proprietary Name
Sulfur
Dosage Form
-
Usage Information
Make lather with sponge.Apply to affected areas.Leave lather on skin for 3 to 5 minutes.Rinse thoroughly with water and gently pat dry with a clean toweI.May be used 1 to 3 times a day or as directed by a doctor Make lather with sponge.Apply to affected areas.Leave lather on skin for 3 to 5 minutes.Rinse thoroughly with water and gently pat dry with a clean toweI.May be used 1 to 3 times a day or as directed by a doctor

Regulatory & Marketing

Labeler Name
Meixin Beauty & Health Care Products Co., Ltd.
FDA Application #
part358H
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
12-25-2021
Listing Expiration
12-31-2023
Exclude Flag
I
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 78565-106-02 identifies a specific commercial package of 240 g in 1 box of Sulfur, labeled by Meixin Beauty & Health Care Products Co., Ltd.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Meixin Beauty & Health Care Products Co., Ltd. on December 25, 2021. The current certification is valid through December 31, 2023.

How is this Meixin Beauty & Health Care Products Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 78565010602. 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)
78565-106-02
11-Digit CMS (5-4-2)
78565-0106-02

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