DERMAREST PSORIASIS MEDICATED- salicylic acid liquid

Dermarest by

Drug Labeling and Warnings

Dermarest by is a Otc medication manufactured, distributed, or labeled by Insight Pharmaceuticals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Salicylic acid 3%

Purposes

Psoriasis and seborrhheic dermatitis treatment

Uses

relieves and helps prevent recurrence of scalp:

• itching
  
• irritation
  
• redness
  
• flaking
  
• scaling

due to psoriasis and seborrheic dermatitis

Warnings

For external use only

Ask a doctor before use if

you have psoriasis that covers a large area of the body

When using this product

avoid contact with the eyes. If contact occurs, rinse the eyes thoroughly with water.

Stop use and ask a doctor if

condition worsens or does not improve after regular use as directed

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• for best results use at least twice a week or as directed by a doctor
  
• wet hair thoroughly
  
• massage liberal amount of product into scalp
  
• leave lather on for several minutes
  
• rinse thoroughly and repeat if needed

Other information

Store at 15° - 25°C (59° – 77°F)

Inactive ingredients

Purified water, ammonium lauryl sulfate, sodium laureth sulfate, sodium citrate, cocamidopropyl betaine, lauryl glucoside, PEG-150 pentaerythrityl tetrastearate, coco-glucoside, glyceryl oleate, aleurites moluccana seed oil, zinc PCA, panthenol, rheum palmatum extract, carthamus tinctorius (safflower) flower extract, camellia sinensis leaf extract, edetate disodium

Questions?

call 1-800-344-7239 dermarest.com

PRINCIPAL DISPLAY PANEL

- 236 ml Bottle Carton

Dermares®
Psoriasis
Salicylic Acid 3%
Psoriasis & Seborrheic Dermatitis Shampoo
Medicated Shampoo + Conditioner
8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

DERMAREST  PSORIASIS MEDICATED
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63736-302
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
KUKUI NUT OIL (UNII: TP11QR7B8R)
ZINC PIDOLATE (UNII: C32PQ86DH4)
PANTHENOL (UNII: WV9CM0O67Z)
RHEUM PALMATUM WHOLE (UNII: 75P857ARCY)
SAFFLOWER (UNII: 4VBL71TY4Y)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Product Characteristics
Color	WHITE (Clear)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63736-302-24	1 in 1 CARTON	07/23/2010
1		236 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part358H	07/23/2010

Labeler - Insight Pharmaceuticals LLC (055665422)