NDC 71819-004 Dermaharmony Sulfur And Salicylic Acid

Salicylic Acid, Sulfur

NDC Product Information

Dermaharmony Sulfur And Salicylic Acid with NDC 71819-004 is a a human over the counter drug product labeled by D3 Development, Inc.. The generic name of Dermaharmony Sulfur And Salicylic Acid is salicylic acid, sulfur. The product's dosage form is soap and is administered via topical form.

Labeler Name: D3 Development, Inc.

Dosage Form: Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.

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 Sulfur And Salicylic Acid 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.

  • SULFUR 5 g/100g
  • SALICYLIC ACID 2 g/100g

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.

  • WATER (UNII: 059QF0KO0R)

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.
  • 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: 07-02-2019 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Dermaharmony Sulfur And Salicylic Acid Product Label Images

Dermaharmony Sulfur And Salicylic Acid 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


Drug Facts

Distributed by:D3 Development, Inc., Portland, ME 04101Made in the USA

Otc - Active Ingredient

Active ingredientsSalicylic acid 2%Sulfur 5%

Otc - Purpose

PurposeDandruff / sebhorreic dermatitis / psoriasis soap

Indications & Usage

Uses​Helps prevent and control recurrence of itching, flaking and irritation associated with dandruff, sebhorreic dermatitis, and psoriasis


WarningsFor external use only

Otc - Ask Doctor

Ask a doctor before use if you have a condition that covers a large area 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 (1-800-222-1222) right away.

Dosage & Administration

  • DirectionsUse on affected areas in place of your regular soap.For best results use at least twice a week or as directed by a doctor.Work up a lather using warm water and massage into affected areas.Rinse.

Storage And Handling

  • Other informationStore at 59° to 77°F (15° to 25°C)Lot number and expiration date are printed on back panel

Inactive Ingredient

Inactive ingredientsSodium palmate, sodium cocoate*, sodium palm kernelate*, water, glycerin, soyethyl morpholinium ethosulfate (soy derived), sodium chloride, pentasodium pentetate*May contain this ingredient

Otc - Questions


* Please review the disclaimer below.