Zo Skin Health Astringent Solution Powder
NDC Package 42851-090-06

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

Package Information

Zo Skin Health Astringent Solution (aluminum acetate) powders is dissolve 1 packet in 12 oz. This formulation utilizes a powder delivery system. Marketed by Zo Skin Health, Inc., this product is identified by NDC 42851-090 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
42851-090-06
Package Description
6 g in 1 PACKET
Product Code
42851-090
11-Digit Billing Format
42851009006

Clinical Specifications

Proprietary Name
Zo Skin Health Astringent Solution
Non-Proprietary Name
Aluminum Acetate
Substance Name
Aluminum Acetate
Dosage Form
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
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)
ALUMINUM ACETATE 4866 mg/6g
Usage Information
Dissolve 1 packet in 12 oz. of cool or warm water.stir until fully dissolved; do not strain or filter.The resulting mixture contains 0.45% aluminum acetate and is ready for use.For use as a compress or wet dressing:soak a clean, soft cloth in the solutionapply cloth loosely to affected area for 15 to 30 minutesrepeat as needed or as directed by a doctordiscard solution after each use

Regulatory & Marketing

Labeler Name
Zo Skin Health, Inc.
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-21-2022
Listing Expiration
12-31-2026
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 42851-090-06 identifies a specific commercial package of 6 g in 1 packet of Zo Skin Health Astringent Solution, a human over the counter drug labeled by Zo Skin Health, Inc.. This powder is formulated for topical use and contains aluminum acetate 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 Zo Skin Health, Inc. on February 21, 2022. The current certification is valid through December 31, 2026.

How is this Zo Skin Health, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 42851009006. 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)
42851-090-06
11-Digit CMS (5-4-2)
42851-0090-06

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