PSORIASIS CREAM- allantoin cream cream

Psoriasis Cream by

Drug Labeling and Warnings

Psoriasis Cream by is a Otc medication manufactured, distributed, or labeled by Kanamed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Allantoin 1%​

INDICATIONS & USAGE

Temporarily protects and helps relieve chapped or cracked skin​

INACTIVE INGREDIENT

• Hemp seed oil
• Shea Butter
• Aloe vera Juice
• Avocado Oil
• Jojoba Extract
• Honey Extract
• Peppermint Extract
• Carrot Seed Oil
• Glycerine
• Stearic Acid
• EDTA
• Arcel 165
• Carbopol U-10,
• Cetyl Alcohol
• BHT
• Cetearyl Alcohol
• Cetearyl Glucoside
• Phenoxyethanol
• Ethylhexlglycerin
• Sorbitan Stearate
• Cyclopentasiloxane
• Phenyl Trimethicone
• Dimethiconol
• C12-15 Alkyl Benzoate
• Dimethicone Crosspolymer
• Caustic Soda/Sodium Hydroxide
• Capric Caprylic Triglyceride
• Polysorbate 60
• Ethylenediaminetetraacetic Acid
• Glycerine
• Carbopol U10
• Caustic Soda/Sodium hydroxide
• Propylene Glycol
• Sodium Benzonate
• DM Water
• Perfume
• Imidaolidnyl Urea

DOSAGE & ADMINISTRATION

Apply as needed

WARNINGS

• For external use only
• When using this product do not get into eyes

STOP use and ask a doctor if:

• Conditions worsens
• symptoms last more than 7 days or clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PURPOSE

Skin Protectant

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PSORIASIS CREAM 
allantoin cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73239-1905
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
HEMP (UNII: TD1MUT01Q7)
WATER (UNII: 059QF0KO0R)	1 mg  in 100 mL
PEPPERMINT (UNII: V95R5KMY2B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73239-1905-1	100 mL in 1 TUBE; Type 0: Not a Combination Product	10/16/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	10/16/2019

Labeler - Kanamed Inc. (117131580)

Registrant - Kanamed Inc. (117131580)