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  5. NDC Package Code: 61734-021-02 Blue Ice Analgesic

NDC Package 61734-021-02 Blue Ice Analgesic

Menthol Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
61734-021-02
Package Description:
113.56 g in 1 CONTAINER
Product Code:
61734-021
Proprietary Name:
Blue Ice Analgesic
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
Usage Information:
See important warnings under "When using this product"adults and children 2 years of age and older:apply liberally to painful area and massage until gel is absorbeduse up to 3-4 times daily or as directed by a doctorchildren under 2 years of age:do not use, unless advised by a physician
11-Digit NDC Billing Format:
61734002102
Product Type:
Human Otc Drug
Labeler Name:
Delon Laboratories (1990) Ltd
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route(s):
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):
MENTHOL 2 g/100g
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-07-2010
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
61734-021-01100 g in 1 BOTTLE, PUMP
61734-021-03227 g in 1 CONTAINER

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 61734-021-02?

The NDC Packaged Code 61734-021-02 is assigned to a package of 113.56 g in 1 container of Blue Ice Analgesic, a human over the counter drug labeled by Delon Laboratories (1990) Ltd. The product's dosage form is gel and is administered via topical form.

Is NDC 61734-021 included in the NDC Directory?

Yes, Blue Ice Analgesic with product code 61734-021 is active and included in the NDC Directory. The product was first marketed by Delon Laboratories (1990) Ltd on May 07, 2010 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 61734-021-02?

The 11-digit format is 61734002102. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-261734-021-025-4-261734-0021-02