DERMAREST PSORIASIS MEDICATED SCALP TREATMENT- salicylic acid gel

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 seborrheic 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 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

apply to affected areas one to four times daily or as directed by a doctor

Other information

Store at room temperature 15°-25°C (59°-77°F).

Inactive ingredients

propylene glycol, purified water, SD alcohol 40, PPG-2 myristyl ether propionate, corn starch modified, zinc PCA, panthenol, aleurites moluccana seed oil, rheum palmatum extract, carthamus tinctorius (safflower) lower extract, camellia sinensis leaf extract, PPG-5-ceteth-20, edetate disodium, xanthan gum, triethanolamine, methylparaben, propylparaben, fragrance

Questions? 

1-800-344-7239 dermarest.com

PRINCIPAL DISPLAY PANEL

DERMAREST®
Psoriasis
SALICYLIC ACID 3%
Psoriasis & Seborrheic Dermatitis Gel

MAX STRENGTH MEDICATED GEL

4 FL OZ (118 mL)

INGREDIENTS AND APPEARANCE

DERMAREST  PSORIASIS MEDICATED SCALP TREATMENT
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63736-312
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
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 4 (UNII: CZ227117JE)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)
BIS-PEG-18 METHYL ETHER DIMETHYL SILANE (UNII: OEB4R3WW9C)
KUKUI NUT OIL (UNII: TP11QR7B8R)
ZINC PIDOLATE (UNII: C32PQ86DH4)
PANTHENOL (UNII: WV9CM0O67Z)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
SAFFLOWER (UNII: 4VBL71TY4Y)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TROLAMINE (UNII: 9O3K93S3TK)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63736-312-24	24 in 1 CASE	12/20/2010
1		1 in 1 CARTON
1		118 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	12/20/2010

Labeler - Insight Pharmaceuticals LLC (055665422)