NDC 73239-1905 Psoriasis Cream

Allantoin Cream

NDC Product Code 73239-1905

NDC 73239-1905-1

Package Description: 100 mL in 1 TUBE

NDC Product Information

Psoriasis Cream with NDC 73239-1905 is a a human over the counter drug product labeled by Kanamed Inc.. The generic name of Psoriasis Cream is allantoin cream. The product's dosage form is cream and is administered via topical form.

Labeler Name: Kanamed Inc.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Psoriasis Cream 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.

  • ALLANTOIN 1 mg/100mL

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: Kanamed Inc.
Labeler Code: 73239
FDA Application Number: part347 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: 10-16-2019 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.

Psoriasis Cream Product Label Images

Psoriasis Cream 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

Otc - Active Ingredient

Allantoin 1%​

Indications & Usage

Temporarily protects and helps relieve chapped or cracked skin​

Inactive Ingredient

  • Hemp seed oilShea ButterAloe vera JuiceAvocado OilJojoba ExtractHoney Extract Peppermint Extract Carrot Seed OilGlycerineStearic AcidEDTAArcel 165Carbopol U-10,Cetyl AlcoholBHTCetearyl AlcoholCetearyl GlucosidePhenoxyethanolEthylhexlglycerinSorbitan StearateCyclopentasiloxanePhenyl TrimethiconeDimethiconolC12-15 Alkyl BenzoateDimethicone CrosspolymerCaustic Soda/Sodium HydroxideCapric Caprylic TriglyceridePolysorbate 60Ethylenediaminetetraacetic AcidGlycerineCarbopol U10Caustic Soda/Sodium hydroxidePropylene GlycolSodium BenzonateDM WaterPerfumeImidaolidnyl Urea

Dosage & Administration

Apply as needed


  • For external use onlyWhen using this product do not get into eyesSTOP use and ask a doctor if:Conditions worsenssymptoms last more than 7 days or clear up and occur again within a few days

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Otc - Purpose

Skin Protectant

* Please review the disclaimer below.