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  5. NDC Package Code: 83509-003-01 Bubble Fade Away Acne Spot Treatment

NDC Package 83509-003-01 Bubble Fade Away Acne Spot Treatment

Benzoyl Peroxide Emulsion 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:
83509-003-01
Package Description:
1 TUBE in 1 CARTON / 10 mL in 1 TUBE
Product Code:
83509-003
Proprietary Name:
Bubble Fade Away Acne Spot Treatment
Non-Proprietary Name:
Benzoyl Peroxide
Substance Name:
Benzoyl Peroxide
Usage Information:
This medication is used to treat mild to moderate acne. It may be used in combination with other acne treatments. When applied to the skin, benzoyl peroxide works by reducing the amount of acne-causing bacteria and by causing the skin to dry and peel. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.
11-Digit NDC Billing Format:
83509000301
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Bubble Beauty
Dosage Form:
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
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):
BENZOYL PEROXIDE 50 mg/mL
Sample Package:
No
FDA Application Number:
M006
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
12-01-2024
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 83509-003-01?

The NDC Packaged Code 83509-003-01 is assigned to a package of 1 tube in 1 carton / 10 ml in 1 tube of Bubble Fade Away Acne Spot Treatment, a human over the counter drug labeled by Bubble Beauty. The product's dosage form is emulsion and is administered via topical form.

Is NDC 83509-003 included in the NDC Directory?

Yes, Bubble Fade Away Acne Spot Treatment with product code 83509-003 is active and included in the NDC Directory. The product was first marketed by Bubble Beauty on December 01, 2024 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 83509-003-01?

The 11-digit format is 83509000301. 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
5-3-283509-003-015-4-283509-0003-01