Chestrub Ointment
NDC Package 20276-100-31

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

Package Information

Chestrub (camphor menthol eucalyptus oil) ointment is usesTemporarily relieves symptoms associated with the common cold:cough  nasal congestionchest congestionTemporarily relieves minor aches and pains of muscles. This formulation utilizes a ointment delivery system. Marketed by Delta Brands Inc, this product is identified by NDC 20276-100 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
20276-100-31
Package Description
113 g in 1 JAR
Product Code
20276-100
11-Digit Billing Format
20276010031
RxNorm Crosswalk
  • RxCUI: 1042786 - camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Ointment
  • RxCUI: 1042786 - camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 MG/MG Topical Ointment

Clinical Specifications

Proprietary Name
Chestrub
Non-Proprietary Name
Camphor Menthol Eucalyptus Oil
Substance Name
Camphor (synthetic); Eucalyptus Oil; Menthol
Dosage Form
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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 relieves symptoms associated with the common cold:cough  nasal congestionchest congestionTemporarily relieves minor aches and pains of muscles

Regulatory & Marketing

Labeler Name
Delta Brands Inc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-15-2009
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 20276-100-31 identifies a specific commercial package of 113 g in 1 jar of Chestrub, a human over the counter drug labeled by Delta Brands Inc. This ointment 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 Delta Brands Inc on November 15, 2009. The current certification is valid through December 31, 2026.

How is this Delta Brands Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 20276010031. 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)
20276-100-31
11-Digit CMS (5-4-2)
20276-0100-31

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