Label: ACNE WASH DAILY CLEANSER- salicylic acid 2.00% liquid

  • 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 March 27, 2018

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  • ACTIVE INGREDIENT

    Active ingredient                                                                     Purpose
    Salicylic Acid 2%......................................................................Acne Treatment

  • PURPOSE

  • Use

    for the treatment of acne

  • WarningsFor external use only.


    Allergy alert: Do not use this product if you have a known allergy to salicylic acid
    When using this product • skin irritation and dryness is more likely to occur
    if you use another topical acne medication at the same time. If irritation
    occurs, only use one topical acne medication at a time. • Avoid contact with
    eyes. If contact occurs, flush thoroughly with water.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a
    Poison Control Center right away

  • Directions

     Cleanse twice a day. • Wet face. • Apply to hands, add
    water and work into lather. • Massage face gently, rinse thoroughly.

  • Inactive ingredients

    Aloe Barbadensis Leaf Extract
    Anthemis Nobilis Flower Extract
    Benzalkonium Chloride
    C12-15 Alkyl Lactate
    Chamomilla Recutita (Matricaria) Flower Extract
    Cocamidopropyl Betaine
    Cocamidopropyl PG-Dimonium Chloride Phosphate
    Disodium EDTA
    Fragrance
    PEG-80 Sorbitan Laurate
    Propylene Glycol
    Red 40
    Sodium C14-16 Olefin Sulfonate
    Water
    Yellow 5

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    ACNE WASH DAILY CLEANSER 
    salicylic acid 2.00% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-7779
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    CHAMOMILE (UNII: FGL3685T2X)  
    Cocamidopropyl PG-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    ALOE (UNII: V5VD430YW9)  
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    C12-15 Alkyl Lactate (UNII: GC844VRD7E)  
    PEG-80 Sorbitan Laurate (UNII: 239B50Y732)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Benzalkonium Chloride (UNII: F5UM2KM3W7)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-7779-5177 mL in 1 BOTTLE; Type 0: Not a Combination Product12/26/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D12/26/2013
    Labeler - Rite Aid (014578892)
    Registrant - Product Quest Mfg (927768135)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg927768135manufacture(11822-7779) , label(11822-7779)
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