Drug Information

Product NDC: 61995-0129

Proprietary Name: J1002901Jason Dandruff Relief 2in1Treatment

Non Proprietary Name: Zinc Pyrithione

Active Ingredient(s):
  • 1 g/100g PYRITHIONE ZINC

Administration Route(s): TOPICAL

Dosage Form(s): SHAMPOO

Labeler Information

Labeler Name: The Hain Celestial Group, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part358H
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:11/27/2017

Package Information

No. Package Code Package Description Billing Unit
161995-0129-8355 g in 1 BOTTLE (61995-0129-8)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61995-0129The 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 NAMEJ1002901Jason Dandruff Relief 2in1TreatmentThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEZinc PyrithioneThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESHAMPOOThe 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 DATE11/27/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct 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 NUMBERpart358HThis 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 NAMEThe Hain Celestial Group, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEPYRITHIONE ZINCThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Download Record

Download this NDC record in Text format: Export

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

Download this NDC record in XML format: Export

This page was last updated on: 8/16/2019