65585-562 NDC - WHISKCARE 362 (CHLOROXYLENOL)

Drug Information

  • Product NDC: 65585-562
  • Proprietary Name: WhiskCare 362
  • Non Proprietary Name: Chloroxylenol
  • Active Ingredient(s): 7.5 mg/mL CHLOROXYLENOL
  • Administration Route(s): TOPICAL
  • Dosage Form(s): SOAP

Labeler Information

Field Name Field Value
Labeler Name: Whisk Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: 505G(a)(3)
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:1/23/2006

Package Information

No. Package Code Package Description Billing Unit
165585-562-0159 mL in 1 TUBE (65585-562-01)
265585-562-0212 BOTTLE, PUMP in 1 BOX (65585-562-02) / 354.9 mL in 1 BOTTLE, PUMP
365585-562-0312 BAG in 1 BOX (65585-562-03) / 800 mL in 1 BAG
465585-562-046 BOTTLE, PUMP in 1 BOX (65585-562-04) / 1750 mL in 1 BOTTLE, PUMP
565585-562-053785 mL in 1 BOTTLE, PLASTIC (65585-562-05)
665585-562-06208198 mL in 1 DRUM (65585-562-06)
765585-562-0710 BAG in 1 BOX (65585-562-07) / 1200 mL in 1 BAG
865585-562-084 BOTTLE, PUMP in 1 BOX (65585-562-08) / 4000 mL in 1 BOTTLE, PUMP
965585-562-0918 BAG in 1 BOX (65585-562-09) / 500 mL in 1 BAG
1065585-562-1012 BOTTLE, PUMP in 1 BOX (65585-562-10) / 236.59 mL in 1 BOTTLE, PUMP
1165585-562-118 BAG in 1 BOX (65585-562-11) / 1000 mL in 1 BAG
1265585-562-1212 BAG in 1 BOX (65585-562-12) / 800 mL in 1 BAG
1365585-562-1359 mL in 1 BOTTLE, PLASTIC (65585-562-13)

NDC Record

Field Name Field Value Definition
PRODUCT NDC65585-562The 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 NAMEHUMAN OTC DRUGIndicates 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 NAMEWhiskCare 362The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEChloroxylenolThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOAPThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/23/2006This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBER505G(a)(3)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 NAMEWhisk Products, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECHLOROXYLENOLAn 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 STRENGTH7.5 
ACTIVE INGRED UNITmg/mL 

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This page was last updated on: 6/6/2025