0363-1740 NDC - PRE-MOISTENED MEDICATED WIPES, PRE-MOISTENED MEDICATED WIPES WITCH HAZEL 50%/HEMORRHOIDAL ASTRINGENT, WALGREENS PRE-MOISTENED MEDICATED WIPES, WALGREENS PRE-MOISTENED MEDICATED WIPES WITCH HAZEL 50%/HEMORRHOIDAL ASTRINGENT (WITCH HAZEL)

Drug Information

Product NDC: 0363-1740
Proprietary Name: Pre-moistened Medicated Wipes, Pre-moistened Medicated Wipes Witch Hazel 50%/Hemorrhoidal Astringent, Walgreens Pre-moistened Medicated Wipes, Walgreens Pre-moistened Medicated Wipes Witch Hazel 50%/Hemorrhoidal Astringent
Non Proprietary Name: Witch Hazel
Active Ingredient(s): 50 mg/100mg WITCH HAZEL
Administration Route(s): TOPICAL
Dosage Form(s): CLOTH

Labeler Information

Field Name	Field Value
Labeler Name:	Walgreens Company
Product Type:	HUMAN OTC DRUG
FDA Application Number:	M015
Marketing Category:	OTC MONOGRAPH DRUG
Start Marketing Date:	4/18/2010

Package Information

No.	Package Code	Package Description	Billing Unit
1	0363-1740-48	48 PATCH in 1 PACKET (0363-1740-48) / 50 mg in 1 PATCH

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	0363-1740	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	HUMAN OTC DRUG	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAME	Pre-moistened Medicated Wipes, Pre-moistened Medicated Wipes Witch Hazel 50%/Hemorrhoidal Astringent, Walgreens Pre-moistened Medicated Wipes, Walgreens Pre-moistened Medicated Wipes Witch Hazel 50%/Hemorrhoidal Astringent	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	Witch Hazel	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	CLOTH	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	TOPICAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	4/18/2010	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	OTC MONOGRAPH DRUG	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBER	M015	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAME	Walgreens Company	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	WITCH HAZEL	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	50
ACTIVE INGRED UNIT	mg/100mg

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 4/4/2025

Previous Code

Next Code