ARCTIVA PSORIASIS CREAM- psoriasis cream cream

Arctiva Psoriasis Cream by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient
Salysilic Acid 2%.........

PURPOSE

Purpose.... Psoriasis

INDICATIONS & USAGE

Uses: Temporarily protects and helps relieve minor skin irritation and itching due to psoriasis.

WARNINGS

Warnings

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

Stop using and ask a doctor if: condition worsen, 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. If swallowed, get medical help or contact a

Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Directions Apply twice daily or as needed.

For best results apply after cleansing.

INACTIVE INGREDIENT

Inactive Ingredients: Water, Cetyl Alcohol,

Stearyl Alcohol, Glyceryl Stearate,

Candelilla/Jojoba/Rice Bran Polyglyceryl- 3

Esters, Sodium Hydroxide, Sodium stearoyl

lactylate, Cetearyl Alcohol, Phenoxyethanol,

Pentylene Glycol, Hydrosurf (Glycolipids),

Hydroxyethylcellulose, Ethylhexyglycerin,

Sodium Ascorbyl Phosphate, Vitamin B3

(Niacinamide), Vitamin A (Retinyl Palmitate),

Tocopherol, Soybean Oil.

STORAGE AND HANDLING

Other Information: Store at room temperature.

QUESTIONS

Questions: 1-833-933-SKIN (7546)

SPL UNCLASSIFIED SECTION

THE ARCTIVA GUARANTEE

Arctiva relief goes beyond the surface. If for any reason

you're not completely satisfied contact us within 60days of your purchase for a

full refund.

Distributed by:

Arctiva Wellness, LLC

30600 Aurora Rd.

Suite 180

Solon, OH 44139

Made in U.S.A

arctivaskin.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARCTIVA PSORIASIS CREAM 
psoriasis cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58418-822
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2.6 g  in 130 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
NIACINAMIDE (UNII: 25X51I8RD4)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
CANDELILLA WAX (UNII: WL0328HX19)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
RICE BRAN (UNII: R60QEP13IC)
LIPID A 504 (UNII: Q2VF73396U)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROXYETHYL CELLULOSE (280 MPA.S AT 2%) (UNII: 12VCE9HR9E)
POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
WATER (UNII: 059QF0KO0R)
CETYL ALCOHOL (UNII: 936JST6JCN)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Product Characteristics
Color	white (lotion)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58418-822-99	1 in 1 CARTON	02/01/2023
1	NDC: 58418-822-45	130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 58418-822-44	1 in 1 CARTON	10/02/2023
2	NDC: 58418-822-40	40 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	02/01/2023

Labeler - Epic Laboratories, LLC (119307904)