Up And Up Liquid
NDC Package 11673-024-54

11-digit billing NDC: 11673002454
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Up And Up (salicylic acid) liquids is • cover the entire affected area with a thin layer and rinse thoroughly one to three times daily • if bothersome dryness or peeling occurs, reduce application to once a day or every other day • 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. This formulation utilizes a liquid delivery system. Marketed by Target Corporation, this product is identified by NDC 11673-024 and is authorized under FDA application M006.

Identification & Billing

NDC Package Code
11673-024-54
Package Description
269.1 mL in 1 BOTTLE, PLASTIC
Product Code
11673-024
11-Digit Billing Format
11673002454
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Up And Up Acne Wash
Non-Proprietary Name
Salicylic Acid
Substance Name
Salicylic Acid
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
SALICYLIC ACID 20 mg/mL
Usage Information
• cover the entire affected area with a thin layer and rinse thoroughly one to three times daily • if bothersome dryness or peeling occurs, reduce application to once a day or every other day • 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.

Regulatory & Marketing

Labeler Name
Target Corporation
Product Type
Human Otc Drug
FDA Application #
M006
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-25-2013
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 11673-024-54 identifies a specific commercial package of 269.1 ml in 1 bottle, plastic of Up And Up Acne Wash, a human over the counter drug labeled by Target Corporation. This liquid is formulated for topical use and contains salicylic acid 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 Target Corporation on October 25, 2013. The current certification is valid through December 31, 2027.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673002454. 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)
11673-024-54
11-Digit CMS (5-4-2)
11673-0024-54

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