5 Day Liquid
NDC Package 69846-110-42

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

Package Information

5 Day (aluminum chlorohydrate) liquids is uses  reduces underarm perspiration. This formulation utilizes a liquid delivery system. Marketed by Numark Brands, Inc, this product is identified by NDC 69846-110 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
69846-110-42
Package Description
75 LIQUID in 1 JAR
Product Code
69846-110
11-Digit Billing Format
69846011042

Clinical Specifications

Proprietary Name
5 Day
Non-Proprietary Name
Aluminum Chlorohydrate
Substance Name
Aluminum Chlorohydrate
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)
ALUMINUM CHLOROHYDRATE .25 g/1
Usage Information
Uses  reduces underarm perspiration

Regulatory & Marketing

Labeler Name
Numark Brands, Inc
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-10-1937
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 69846-110-42 identifies a specific commercial package of 75 liquid in 1 jar of 5 Day, a human over the counter drug labeled by Numark Brands, Inc. This liquid is formulated for topical use and contains aluminum chlorohydrate 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 Numark Brands, Inc on April 10, 1937. The current certification is valid through December 31, 2026.

How is this Numark Brands, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69846011042. 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)
69846-110-42
11-Digit CMS (5-4-2)
69846-0110-42

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