Chloraseptic Sore Throat Menthol Spray
NDC Package 67172-113-31

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Chloraseptic Sore Throat Menthol (phenol) sprays is adults and children 3 years of age and older:Apply to the affected area (one spray). This formulation utilizes a spray delivery system. Marketed by Prestige Brands Holdings, Inc., this product is identified by NDC 67172-113 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
67172-113-31
Package Description
177 mL in 1 BOTTLE, SPRAY
Product Code
11-Digit Billing Format
67172011331
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Chloraseptic Sore Throat Menthol
Non-Proprietary Name
Phenol
Substance Name
Phenol
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
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 dentist. 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 dentist. 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 dentist.

Regulatory & Marketing

Labeler Name
Prestige Brands Holdings, Inc.
Product Type
Human Otc Drug
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2010
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 67172-113-31 identifies a specific commercial package of 177 ml in 1 bottle, spray of Chloraseptic Sore Throat Menthol, a human over the counter drug labeled by Prestige Brands Holdings, Inc.. This spray is formulated for oral 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 Prestige Brands Holdings, Inc. on September 01, 2010. The current certification is valid through December 31, 2026.

How is this Prestige Brands Holdings, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 67172011331. 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)
67172-113-31
11-Digit CMS (5-4-2)
67172-0113-31

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