Skinuva Bruise Capsule
NDC Package 82350-001-14

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Skinuva Bruise (arnica montana, bromelain, grape seed extract, vitamin c, rutin, zinc oxide, cellulose) capsules is uses Reduces pain, swelling, and discoloration from bruises.Temporarily relieves muscle pain and stiffness due to surgery and injury. This formulation utilizes a capsule delivery system. Marketed by Md Medical Designs, Inc., this product is identified by NDC 82350-001.

Identification & Billing

NDC Package Code
82350-001-14
Package Description
14 CAPSULE in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
82350000114

Clinical Specifications

Proprietary Name
Skinuva Bruise
Non-Proprietary Name
Arnica Montana, Bromelain, Grape Seed Extract, Vitamin C, Rutin, Zinc Oxide, Cellulose
Substance Name
Arnica Montana
Dosage Form
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Uses Reduces pain, swelling, and discoloration from bruises.Temporarily relieves muscle pain and stiffness due to surgery and injury.

Regulatory & Marketing

Labeler Name
Md Medical Designs, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
04-10-2023
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 82350-001-14 identifies a specific commercial package of 14 capsule in 1 bottle, plastic of Skinuva Bruise, a human over the counter drug labeled by Md Medical Designs, Inc.. This capsule is formulated for oral use and contains arnica montana 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 Md Medical Designs, Inc. on April 10, 2023. The current certification is valid through December 31, 2027.

How is this Md Medical Designs, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82350000114. 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)
82350-001-14
11-Digit CMS (5-4-2)
82350-0001-14

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