The Pharma C Company Medicated Foam With Witch Hazel Liquid
NDC Package 55239-358-00
Package Information
The Pharma C Company Medicated Foam With Witch Hazel (witch hazel) liquids is adults: when practical, clean the affected area with mild soap and warm water and rinse thoroughlygently dry area by patting or blotting with toilet tissure or a soft clothpump a small amount of foam onto clean toilet paper and apply externally to the affected areaafter application, flush toilet paper and wash handsmedicated foam may be used up to 6 times daily or after each bowel movement Children under 12 years of age: ask a doctor. This formulation utilizes a liquid delivery system. Marketed by Kleen Test Products Corporation, this product is identified by NDC 55239-358 and is authorized under FDA application M015.
Identification & Billing
- RxCUI: 2166922 - witch hazel 50 % Topical Foam
- RxCUI: 2166922 - witch hazel 500 MG/ML Topical Foam
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 55239 - Kleen Test Products Corporation
- 55239-358 - The Pharma C Company Medicated Foam With Witch Hazel
- 55239-358-00 - 210 mL in 1 BOTTLE
- 55239-358 - The Pharma C Company Medicated Foam With Witch Hazel
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 55239-358-00 identifies a specific commercial package of 210 ml in 1 bottle of The Pharma C Company Medicated Foam With Witch Hazel, a human over the counter drug labeled by Kleen Test Products Corporation. This liquid is formulated for topical use and contains witch hazel 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 Kleen Test Products Corporation on May 15, 2022. The current certification is valid through December 31, 2026.
How is this Kleen Test Products Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 55239035800. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.