Tn Dickinsons Witch Hazel Astringent Liquid
NDC Package 52651-001-06

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

Tn Dickinsons Witch Hazel Astringent (witch hazel) liquids is remove protective inner sealmoisten cotton ball or cleansing pad and gently wipe skinapply as often as necessary. This formulation utilizes a liquid delivery system. Marketed by Dickinson Brands Inc., this product is identified by NDC 52651-001 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
52651-001-06
Package Description
473 mL in 1 BOTTLE, DISPENSING
Product Code
52651-001
11-Digit Billing Format
52651000106
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Tn Dickinsons Witch Hazel Astringent
Non-Proprietary Name
Witch Hazel
Substance Name
Witch Hazel
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
WITCH HAZEL 86 g/100mL
Usage Information
Remove protective inner sealmoisten cotton ball or cleansing pad and gently wipe skinapply as often as necessary

Regulatory & Marketing

Labeler Name
Dickinson Brands Inc.
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-02-1989
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 (52651-001). Click a package code to view its specific billing and regulatory data.

52651-001-04
3785 mL in 1 BOTTLE
52651-001-05
237 mL in 1 BOTTLE, DISPENSING
52651-001-07
59 mL in 1 BOTTLE

* 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 52651-001-06 identifies a specific commercial package of 473 ml in 1 bottle, dispensing of Tn Dickinsons Witch Hazel Astringent, a human over the counter drug labeled by Dickinson Brands Inc.. 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 Dickinson Brands Inc. on December 02, 1989. The current certification is valid through December 31, 2026.

How is this Dickinson Brands Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52651000106. 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)
52651-001-06
11-Digit CMS (5-4-2)
52651-0001-06

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