Biocence Spray
NDC Package 59998-202-10

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

Biocence (eucalyptol thymol) sprays is cLEAN THE AFFECTED AREA.APPLY A SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1 TO 3 TIMES DAILY.BANDAGE LIGHTLY.KEEP BANDAGE WET WITH SOLUTION.SPRAY A SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1 TO 3 TIMES DAILY.MAY BE COVERED WITH STERILE BANDAGE.IF BANDAGED, LET DRY FIRST. This formulation utilizes a spray delivery system. Marketed by Bio-germ Protection Llc, this product is identified by NDC 59998-202.

Identification & Billing

NDC Package Code
59998-202-10
Package Description
10 mL in 1 BOTTLE, GLASS
Product Code
59998-202
11-Digit Billing Format
59998020210

Clinical Specifications

Proprietary Name
Biocence
Non-Proprietary Name
Eucalyptol Thymol
Substance Name
Eucalyptol; Thymol
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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
CLEAN THE AFFECTED AREA.APPLY A SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1 TO 3 TIMES DAILY.BANDAGE LIGHTLY.KEEP BANDAGE WET WITH SOLUTION.SPRAY A SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1 TO 3 TIMES DAILY.MAY BE COVERED WITH STERILE BANDAGE.IF BANDAGED, LET DRY FIRST.

Regulatory & Marketing

Labeler Name
Bio-germ Protection Llc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
10-26-2012
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (59998-202). Click a package code to view its specific billing and regulatory data.

59998-202-12
50 mL in 1 BOTTLE, GLASS
59998-202-13
100 mL in 1 BOTTLE, GLASS
59998-202-14
118 mL in 1 BOTTLE, SPRAY
59998-202-32
946 mL in 1 BOTTLE
59998-202-64
1893 mL in 1 JUG

* 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 59998-202-10 identifies a specific commercial package of 10 ml in 1 bottle, glass of Biocence, a human over the counter drug labeled by Bio-germ Protection Llc. This spray is formulated for topical use and contains eucalyptol; thymol 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 Bio-germ Protection Llc on October 26, 2012. The current certification is valid through December 31, 2026.

How is this Bio-germ Protection Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59998020210. 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)
59998-202-10
11-Digit CMS (5-4-2)
59998-0202-10

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