Hand Antiperspirant Daily Use Cream
NDC Package 74307-007-01

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

Package Information

Hand Antiperspirant Daily Use (aluminum zirconium octachlorohydrex gly) cream is stop use if rash or irritation occurs. This formulation utilizes a cream delivery system. Marketed by Clutch Inc, this product is identified by NDC 74307-007 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
74307-007-01
Package Description
30 mL in 1 BOTTLE, PUMP
Product Code
74307-007
11-Digit Billing Format
74307000701

Clinical Specifications

Proprietary Name
Hand Antiperspirant Daily Use
Non-Proprietary Name
Aluminum Zirconium Octachlorohydrex Gly
Substance Name
Aluminum Zirconium Octachlorohydrex Gly
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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 ZIRCONIUM OCTACHLOROHYDREX GLY 20 g/100mL
Usage Information
Stop use if rash or irritation occurs

Regulatory & Marketing

Labeler Name
Clutch Inc
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-01-2020
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 74307-007-01 identifies a specific commercial package of 30 ml in 1 bottle, pump of Hand Antiperspirant Daily Use, a human over the counter drug labeled by Clutch Inc. This cream is formulated for topical use and contains aluminum zirconium octachlorohydrex gly 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 Clutch Inc on June 01, 2020. The current certification is valid through December 31, 2027.

How is this Clutch Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 74307000701. 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)
74307-007-01
11-Digit CMS (5-4-2)
74307-0007-01

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