Kinkan Cool Liniment
NDC Package 51027-0330-2

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

Package Information

Kinkan Cool (diphenhydramine hydrochloride, menthol) liniments is adults and children 6 years of age and older: Apply to affected area not more than 3 to 4 times daily. This formulation utilizes a liniment delivery system. Marketed by Kinkando Co., Ltd ., this product is identified by NDC 51027-0330 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
51027-0330-2
Package Description
96 BOX in 1 CARTON / 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE
Product Code
51027-0330
11-Digit Billing Format
51027033002
RxNorm Crosswalk
  • RxCUI: 1298287 - diphenhydrAMINE HCl 2 % / menthol 1 % Topical Solution
  • RxCUI: 1298287 - diphenhydramine hydrochloride 20 MG/ML / menthol 10 MG/ML Topical Solution
  • RxCUI: 1298287 - diphenhydramine hydrochloride 2 % / menthol 1 % Topical Solution

Clinical Specifications

Proprietary Name
Kinkan Cool
Non-Proprietary Name
Diphenhydramine Hydrochloride, Menthol
Substance Name
Diphenhydramine Hydrochloride; Menthol
Dosage Form
Liniment - A solution or mixture of various substances in oil, alcoholic solutions of soap, or emulsions intended for external application.
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)
Pharmacologic Class
Usage Information
Adults and children 6 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 6 years of age: Do not use, consult a doctor.

Regulatory & Marketing

Labeler Name
Kinkando Co., Ltd .
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-26-2000
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 51027-0330-2 identifies a specific commercial package of 96 box in 1 carton / 1 bottle in 1 box / 50 ml in 1 bottle of Kinkan Cool, a human over the counter drug labeled by Kinkando Co., Ltd .. This liniment is formulated for topical use and contains diphenhydramine hydrochloride; menthol 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 Kinkando Co., Ltd . on April 26, 2000. The current certification is valid through December 31, 2026.

How is this Kinkando Co., Ltd . product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51027033002. 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 (5-4-1)
51027-0330-2
11-Digit CMS (5-4-2)
51027-0330-02

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