Germa Camphor Ointment
NDC Package 73635-5809-2

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

Package Information

Germa Camphor (camphor 10%) ointment is do not use • on children • on irritated skin • in or near eyes or mucous membranes • on wounds or damaged skin • if prone to allergic reaction from any of the ingredient • on large areas of the body. This formulation utilizes a ointment delivery system. Marketed by Germa Products, Llc, this product is identified by NDC 73635-5809 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
73635-5809-2
Package Description
56.69 mL in 1 JAR
Product Code
73635-5809
11-Digit Billing Format
73635580902
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Germa Camphor Analgesic
Non-Proprietary Name
Camphor 10%
Substance Name
Camphor (synthetic)
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)
CAMPHOR (SYNTHETIC) 100 mg/mL
Usage Information
Do not use • on children • on irritated skin • in or near eyes or mucous membranes • on wounds or damaged skin • if prone to allergic reaction from any of the ingredient • on large areas of the body. • if you are taking any other medication or drinking alcohol • if safety seal is torn, broken or missing.

Regulatory & Marketing

Labeler Name
Germa Products, Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-29-2019
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 73635-5809-2 identifies a specific commercial package of 56.69 ml in 1 jar of Germa Camphor Analgesic, a human over the counter drug labeled by Germa Products, Llc. This ointment is formulated for topical use and contains camphor (synthetic) 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 Germa Products, Llc on March 29, 2019. The current certification is valid through December 31, 2026.

How is this Germa Products, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73635580902. 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)
73635-5809-2
11-Digit CMS (5-4-2)
73635-5809-02

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