Hand Recovery Lotion
NDC Package 70741-007-01

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

Package Information

Hand Recovery (alcohol) lotions is apply lotion directly onto body and rub with hands until dry. This formulation utilizes a lotion delivery system. Marketed by Derma Glove, this product is identified by NDC 70741-007 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
70741-007-01
Package Description
25 mL in 1 PACKAGE
Product Code
70741-007
11-Digit Billing Format
70741000701
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hand Recovery
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • 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)
Usage Information
Apply lotion directly onto body and rub with hands until dry. Product may be used on all skin surfaces. Children under 6 years of age should be supervised when using this product.

Regulatory & Marketing

Labeler Name
Derma Glove
Product Type
Human Otc Drug
FDA Application #
part333A
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-06-2017
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (70741-007). Click a package code to view its specific billing and regulatory data.

70741-007-02
40 mL in 1 PACKAGE
70741-007-03
75 mL in 1 PACKAGE
70741-007-04
236.8 mL in 1 PACKAGE
70741-007-05
473.6 mL in 1 PACKAGE
70741-007-06
947.2 mL in 1 PACKAGE

* 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 70741-007-01 identifies a specific commercial package of 25 ml in 1 package of Hand Recovery, a human over the counter drug labeled by Derma Glove. This lotion is formulated for topical use and contains alcohol 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 Derma Glove on January 06, 2017. The current certification is valid through December 31, 2026.

How is this Derma Glove product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70741000701. 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)
70741-007-01
11-Digit CMS (5-4-2)
70741-0007-01

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