Label: DERMAREST PSORIASIS MEDICATED- salicylic acid liquid

  • NDC Code(s): 63736-302-24
  • Packager: Insight Pharmaceuticals LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 10, 2020

If you are a consumer or patient please visit this version.

  • 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)

    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 TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-302
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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
    ColorWHITE (Clear) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63736-302-241 in 1 CARTON07/23/2010
    1236 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart358H07/23/2010
    Labeler - Insight Pharmaceuticals LLC (055665422)