NDC 71819-016 Dermaharmony Zinc Therapy

Pyrithione Zinc

NDC Product Code 71819-016

NDC 71819-016-04

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC 71819-016-10

Package Description: 296 mL in 1 BOTTLE, PLASTIC

NDC 71819-016-12

Package Description: 355 mL in 1 BOTTLE, PLASTIC

NDC 71819-016-64

Package Description: 1893 mL in 1 BOTTLE, PLASTIC

NDC 71819-016-99

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Dermaharmony Zinc Therapy with NDC 71819-016 is a a human over the counter drug product labeled by D3 Development, Inc.. The generic name of Dermaharmony Zinc Therapy is pyrithione zinc. The product's dosage form is liquid and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1048123.

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.

Product Type: Human Otc Drug 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.

Dermaharmony Zinc Therapy Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
  • WATER (UNII: 059QF0KO0R)
  • COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
  • SOYETHYL MORPHOLINIUM ETHOSULFATE (UNII: J8C5W5HH18)
  • DISTEARYL PHTHALAMIC ACID (UNII: 5552GSZ9LI)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
  • SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)

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.

Labeler Name: D3 Development, Inc.
Labeler Code: 71819
FDA Application Number: part358H 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: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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.

Start Marketing Date: 09-05-2021 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: 12-31-2022 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: N - NO 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".

* Please review the disclaimer below.

Dermaharmony Zinc Therapy Product Label Images

Dermaharmony Zinc Therapy Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Other

Drug Facts

Distributed by: D3 Development, Inc., Portland, ME 04101Made in USA from U.S. and imported ingredients

Otc - Active Ingredient

Active ingredientPyrithione zinc 2%

Otc - Purpose

PurposesDandruff, Seborrheic dermatitis

Indications & Usage

UsesControls, reduces, and helps stop the symptoms of dandruff and seborrheic dermatitis.

Warnings

WarningsFor external use only

Otc - Ask Doctor

Ask a doctor before use if you have seborrheic dermatitis that covers a large portion of the body

Otc - When Using

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if condition worsens or does not improve after regular use as directed.

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

  • DirectionsShake before each useUse on affected areas in place of your regular soapFor best results use at least twice a week or as directed by a doctorWork up a lather using warm water and massage into affected areasRinse well

Storage And Handling

  • Other informationStore at room temperatureLot number and expiration date on bottom

Inactive Ingredient

Inactive ingredientsWater, Lauryl Glucoside, Cocamidopropyl Hydroxysultaine, Sodium Lauroamphoacetate, Distearyl Phthalic Acid Amide, Sodium Chloride, Lauramine Oxide, Melaleuca Alternifolia (Tea Tree) Oil, Soyethyl Morpholinium Ethosulfate, Phenoxyethanol, Aloe Barbadensis Leaf Juice

Otc - Questions

Questions?1-800-827-3730

* Please review the disclaimer below.