NDC 62839-6745 Epoch Ava Puhi Moni Anti-dandruff
Pyrithione Zinc Shampoo Topical

Product Information

What is NDC 62839-6745?

The NDC code 62839-6745 is assigned by the FDA to the product Epoch Ava Puhi Moni Anti-dandruff which is a human over the counter drug product labeled by Nse Products, Inc.. The generic name of Epoch Ava Puhi Moni Anti-dandruff is pyrithione zinc. The product's dosage form is shampoo and is administered via topical form. The product is distributed in a single package with assigned NDC code 62839-6745-1 250 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code62839-6745
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Epoch Ava Puhi Moni Anti-dandruff
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Pyrithione Zinc
Product Type What kind of product is this?
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.
Human Otc Drug
Dosage FormShampoo - A liquid soap or detergent used to clean the hair and scalp and is often used as a vehicle for dermatologic agents.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Nse Products, Inc.
Labeler Code62839
FDA Application Number What is the FDA Application Number?
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.
Marketing Category What is the Marketing Category?
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.
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
NDC Code Structure

What are the uses for Epoch Ava Puhi Moni Anti-dandruff?

Product Packages

NDC Code 62839-6745-1

Package Description: 250 mL in 1 BOTTLE, PLASTIC

Product Details

What are Epoch Ava Puhi Moni Anti-dandruff Active Ingredients?

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.

Epoch Ava Puhi Moni Anti-dandruff Active Ingredients UNII Codes

Epoch Ava Puhi Moni Anti-dandruff Inactive Ingredients UNII Codes

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

* Please review the disclaimer below.

Epoch Ava Puhi Moni Anti-dandruff Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents


Drug Facts

  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Active Ingredients

Zinc Pyrithione 1%




Controls the symptoms of dandruff.


  • For external use only

Otc - Keep Out Of Reach Of Children

  • Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Otc - Ask Doctor

  • If condition worsens or does not improve after regular use of the product as directed, consult a doctor.


  • Wet hair, lather thoroughly
  • Leave in 1–2 minutes and rinse well
  • For best results, use daily or at least twice a week (or as directed by a doctor).

Inactive Ingredients

Water (Aqua), Ammonium Lauryl Sulfate, Ammonium Laureth Sulfate, Cocamide MIPA, Dimethicone, Zingiber Zerumbet Juice, Clematis Vitalba Leaf Extract, Mahonia Aquifolium Root Extract, Salvia Officinalis (Sage) Leaf Extract, Urtica Dioica (Nettle) Extract, Melia Azadirachta Leaf Extract, Panthenol, Butylene Glycol, Trisodium Ethylenediamine Disuccinate, Acrylates Copolymer, PEG/PPG-18/18 Dimethicone, Hexylene Glycol, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Citric Acid, Sodium Hydroxide, Fragrance (Parfum).



Principal Display Panel - 250 Ml Bottle Label


Ava puhi moni®


the "true ava puhi"

250 ml e (8.4 fl. oz.)

* Please review the disclaimer below.