Goodsense Maximum Strength Medicated Cloth
NDC Package 50804-211-48
Package Information
Goodsense Maximum Strength Medicated (witch hazel) cloths is adult: unfold wipe and cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area.use up to 6 times daily or after each bowel movement and before applying hemorrhoidal treatments, and then discardchildren under 12 years of age:Consult a doctorDispose of wipe in trash.do not flush. This formulation utilizes a cloth delivery system. Marketed by Geiss, Destin & Dunn, Inc, this product is identified by NDC 50804-211 and is authorized under FDA application M016.
Identification & Billing
- RxCUI: 844379 - witch hazel 50 % Medicated Pad
- RxCUI: 844379 - witch hazel 500 MG/ML Medicated Pad
- RxCUI: 844379 - witch hazel 50 % Medicated Wipes
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 50804 - Geiss, Destin & Dunn, Inc
- 50804-211 - Goodsense Maximum Strength Medicated
- 50804-211-48 - 48 PACKET in 1 PACKAGE / 2.9 g in 1 PACKET
- 50804-211 - Goodsense Maximum Strength Medicated
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 50804-211-48 identifies a specific commercial package of 48 packet in 1 package / 2.9 g in 1 packet of Goodsense Maximum Strength Medicated, a human over the counter drug labeled by Geiss, Destin & Dunn, Inc. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package. This cloth 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 Geiss, Destin & Dunn, Inc on July 27, 2017. The current certification is valid through December 31, 2026.
How is this Geiss, Destin & Dunn, Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 50804021148. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 total billable units per package. 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.