Relieveit Spraingo Gel
NDC Package 58133-950-37

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Relieveit Spraingo Gel is adults and children 2 years and over:Shake well before using •Apply a sufficientamount of RelieveIt® SprainGo Gel to cover theaffected area • Repeat as needed • Afterapplying, wash hands with soap and waterChildren under 2: consult a doctor. Marketed by Cosmetic Specialty Labs, Inc., this product is identified by NDC 58133-950.

Identification & Billing

NDC Package Code
58133-950-37
Package Description
3780 mL in 1 BOTTLE, PUMP
Product Code
58133-950
11-Digit Billing Format
58133095037

Clinical Specifications

Proprietary Name
Relieveit Spraingo Gel
Dosage Form
-
Usage Information
Adults and children 2 years and over:Shake well before using •Apply a sufficientamount of RelieveIt® SprainGo Gel to cover theaffected area • Repeat as needed • Afterapplying, wash hands with soap and waterChildren under 2: consult a doctor

Regulatory & Marketing

Labeler Name
Cosmetic Specialty Labs, Inc.
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
10-17-2018
Listing Expiration
12-31-2023
Exclude Flag
I
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 (58133-950). Click a package code to view its specific billing and regulatory data.

58133-950-02
70 mL in 1 BOTTLE, PUMP
58133-950-16
474 mL in 1 BOTTLE, PUMP

* 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 58133-950-37 identifies a specific commercial package of 3780 ml in 1 bottle, pump of Relieveit Spraingo Gel, labeled by Cosmetic Specialty Labs, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Cosmetic Specialty Labs, Inc. on October 17, 2018. The current certification is valid through December 31, 2023.

How is this Cosmetic Specialty Labs, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 58133095037. 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)
58133-950-37
11-Digit CMS (5-4-2)
58133-0950-37

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