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  5. NDC Package Code: 70707-440-15 Sulfur Spot Treatment

NDC Package 70707-440-15 Sulfur Spot Treatment

Sulfur Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
70707-440-15
Package Description:
1 TUBE in 1 BOX / 44 mL in 1 TUBE
Product Code:
70707-440
Proprietary Name:
Sulfur Spot Treatment
Non-Proprietary Name:
Sulfur
Substance Name:
Sulfur
Usage Information:
Clean the skin thoroughly before applying this productcover the entire affected area with a thin layer one to three times dailybecause 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 doctorif bothersome dryness or peeling occurs, reduce application to once a day or every other day
11-Digit NDC Billing Format:
70707044015
NDC to RxNorm Crosswalk:
  • RxCUI: 2273805 - sulfur 6 % Topical Gel
  • RxCUI: 2273805 - sulfur 0.06 MG/MG Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Face Reality, 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):
  • SULFUR 60 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    M006
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-08-2020
    Listing Expiration Date:
    12-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70707-440-04118 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70707-440-15?

    The NDC Packaged Code 70707-440-15 is assigned to a package of 1 tube in 1 box / 44 ml in 1 tube of Sulfur Spot Treatment, a human over the counter drug labeled by Face Reality, Inc. The product's dosage form is gel and is administered via topical form.

    Is NDC 70707-440 included in the NDC Directory?

    Yes, Sulfur Spot Treatment with product code 70707-440 is active and included in the NDC Directory. The product was first marketed by Face Reality, Inc on January 08, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70707-440-15?

    The 11-digit format is 70707044015. 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
    5-3-270707-440-155-4-270707-0440-15