Chest Rub Gel
NDC Package 52920-133-48

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

Package Information

Chest Rub (menthol and camphor and eucalyptus oil) gel is usesTemporarily releives symptoms associated with the common cold: cough nasal congestionchest congestionTemporarily relives minor aches and pains of muscles. This formulation utilizes a gel delivery system. Marketed by Singhfam Corporation, this product is identified by NDC 52920-133 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
52920-133-48
Package Description
113 g in 1 BOTTLE, PLASTIC
Product Code
52920-133
11-Digit Billing Format
52920013348
RxNorm Crosswalk
  • RxCUI: 1547992 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Gel
  • RxCUI: 1547992 - camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical Gel

Clinical Specifications

Proprietary Name
Chest Rub Vaporizing Action
Non-Proprietary Name
Menthol And Camphor And Eucalyptus Oil
Substance Name
Camphor (synthetic); Eucalyptus Oil; Menthol
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
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
UsesTemporarily releives symptoms associated with the common cold: cough nasal congestionchest congestionTemporarily relives minor aches and pains of muscles.

Regulatory & Marketing

Labeler Name
Singhfam Corporation
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-10-2015
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 52920-133-48 identifies a specific commercial package of 113 g in 1 bottle, plastic of Chest Rub Vaporizing Action, a human over the counter drug labeled by Singhfam Corporation. This gel is formulated for topical use and contains camphor (synthetic); eucalyptus oil; 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 Singhfam Corporation on August 10, 2015. The current certification is valid through December 31, 2026.

How is this Singhfam Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52920013348. 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)
52920-133-48
11-Digit CMS (5-4-2)
52920-0133-48

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