Label: TRIDERMA PSORIASIS CONTROL- salicylic acid shampoo

  • NDC Code(s): 10738-980-50, 10738-980-55, 10738-980-82
  • Packager: Genuine Virgin Aloe Corporation
  • 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 February 2, 2023

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  • Drug Facts 

  • Active ingredient

    Salicylic Acid 3.0%

  • Purpose

    Control of Psoriasis, Dermatitis

  • INDICATIONS & USAGE

    Uses Relieves and helps prevent recurrence of: •itching •irritation •redness •flaking •scaling due to psoriasis and seborrheic dermatitis

  • WARNINGS

    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 eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if •condition worsens or does not improve after regular use.

    Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions Use at least twice a week or as directed by a doctor. Wet hair, apply and massage into scalp. Leave on for several minutes. Rinse thoroughly.

  • INACTIVE INGREDIENT

    Inactive ingredients: water, sodium C14-16 olefin sulfonate, cocamidopropyl betaine, urea, glycol distearate, polyquaternium-7, colloidal oatmeal / avena sativa (oat) kernel flour, aloe barbadensis leaf juice*, oenothera biennis (evening primrose) oil, helianthus annuus (sunflower) seed oil, glycerin, glycyrrhiza glabra (licorice) root extract, tocopheryl acetate (vitamin E), panthenol (pro-vitamin B5), allantoin, zinc PCA, piroctone olamine, PEG-150 distearate, sodium citrate, acrylates crosspolymer-4, PEG-12, methyl glucose trioleate, phenoxyethanol, ethylhexylglycerin. *Certified Organic Ingredient - Mayacert Certifier

  • QUESTIONS

    Questions? 1-800-279-7282 M-F 8am-4pm PST

  • SPL UNCLASSIFIED SECTION

    Relieves & helps prevent recurrence of itching, flaking & scaling

    • AP4 ® BOTANICAL •  ALOE VERA COMPLEX

    Psoriasis & Seborrheic Dermatitis

    EXPERTS IN SKIN HEALING SINCE 1992

    Psoriasis Control ® Shampoo  contains clinically proven ingredients that help soothe and relieve psoriasis symptoms.

    • Gentle on hair
    • Relieves dry, itchy scalp & flaking
    • Leaves hair silky soft

    No Steroids, Coal Tar or Cortisone Paraben & SLS Free

    • Soothes dry, itchy scalp

    • Relieves redness & flaking

    QUALITY YOU CAN FEEL

    RESULTS YOU CAN SEE. ®

    TriDerma MD ® provides healing solutions for irritated skin without harmful side effects. 

    www.triderma.com

    Dist. by: Genuine Virgin Aloe Corp.,
    Corona, CA 92879  © 2019
    MADE IN THE USA

  • Packaging

    untitled

  • INGREDIENTS AND APPEARANCE
    TRIDERMA PSORIASIS CONTROL 
    salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10738-980
    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)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    (1,1-DIMETHYLETHYL)UREA (UNII: T81TP489AF)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
    OATMEAL (UNII: 8PI54V663Y)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ZINC PIDOLATE (UNII: C32PQ86DH4)  
    PIROCTONE OLAMINE (UNII: A4V5C6R9FB)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)  
    METHYL GLUCOSE DIOLEATE (UNII: FA9KFJ4Z6P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10738-980-501 in 1 CARTON01/15/2020
    1NDC:10738-980-5515 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:10738-980-82245 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H01/15/2020
    Labeler - Genuine Virgin Aloe Corporation (961374147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Genuine Virgin Aloe Corporation961374147manufacture(10738-980)
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