Phenol Spray
NDC Package 83324-031-06

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

Package Information

Phenol sprays is adults and children 3 years of age and older.Apply to the affected area (one spray) Allow to remain in place for at least 15 seconds, then spit out Use every 2 hours or as directed by a doctor or dentist. This formulation utilizes a spray delivery system. Marketed by Chain Drug Marketing Association Inc., this product is identified by NDC 83324-031 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
83324-031-06
Package Description
177 mL in 1 BOTTLE, SPRAY
Product Code
83324-031
11-Digit Billing Format
83324003106

Clinical Specifications

Proprietary Name
Phenol
Non-Proprietary Name
Phenol
Substance Name
Phenol
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Nasal - Administration to the nose; administered by way of the nose.
Active Ingredient(s)
PHENOL 14 mg/100mL
Usage Information
Adults and children 3 years of age and older.Apply to the affected area (one spray) Allow to remain in place for at least 15 seconds, then spit out Use every 2 hours or as directed by a doctor or dentist. Children under 12 years of age should be supervised in the use of this product. Children under 3 years of age, consult a doctor or dentistBefore using the first time, remove the protective neck band and dust cap from the tip. To spray hold bottle straight up and press thenozzle with index finger without tilting head. Fully depress pump all the way down with a firm, even stroke. Wipe nozzle dry.

Regulatory & Marketing

Labeler Name
Chain Drug Marketing Association Inc.
Product Type
Human Otc Drug
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-12-2024
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 83324-031-06 identifies a specific commercial package of 177 ml in 1 bottle, spray of Phenol, a human over the counter drug labeled by Chain Drug Marketing Association Inc.. This spray is formulated for nasal use and contains phenol 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 Chain Drug Marketing Association Inc. on December 12, 2024. The current certification is valid through December 31, 2026.

How is this Chain Drug Marketing Association Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83324003106. 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)
83324-031-06
11-Digit CMS (5-4-2)
83324-0031-06

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