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  5. NDC Package Code: 85439-0102-1 Sulfur Spot Treatment

NDC Package 85439-0102-1 Sulfur Spot Treatment

Sulfur Acne Treatment Cream 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:
85439-0102-1
Package Description:
15 mL in 1 TUBE
Product Code:
85439-0102
Proprietary Name:
Sulfur Spot Treatment
Non-Proprietary Name:
Sulfur Acne Treatment
Substance Name:
Sulfur
Usage Information:
DirectionsClean the skin thoroughly before applying this product.Cover the entire affected area with a thin layer one to three times daily.Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
11-Digit NDC Billing Format:
85439010201
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Banuskin, Inc.
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):
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):
SULFUR 10 g/100mL
Sample Package:
No
FDA Application Number:
M006
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
04-15-2025
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 85439-0102-1?

The NDC Packaged Code 85439-0102-1 is assigned to a package of 15 ml in 1 tube of Sulfur Spot Treatment, a human over the counter drug labeled by Banuskin, Inc.. The product's dosage form is cream and is administered via topical form.

Is NDC 85439-0102 included in the NDC Directory?

Yes, Sulfur Spot Treatment with product code 85439-0102 is active and included in the NDC Directory. The product was first marketed by Banuskin, Inc. on April 15, 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 85439-0102-1?

The 11-digit format is 85439010201. 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
5-4-185439-0102-15-4-285439-0102-01