Label: OKAY FACIAL SCRUB- salicylic acid gel

  • NDC Code(s): 74553-016-01
  • Packager: Xtreme Tools International, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 30, 2024

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  • Drug Facts

  • Active Ingredient

    Salicylic Acid (2%)

  • Purpose

    Acne Treatment

  • Use

    For the treatment of acne.

  • Warning

    For External use only

  • 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 medication at a time. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    ■ clean the skin thoroughly before applying this product

    ■ cover the entire affected area with a thin layer one to three times daily

    ■ because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor

    ■ if bothersome dryness or peeling occurs, reduce application to once a day or every other day

  • Inactive Ingredients

    Water (Aqua), Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Decyl Glucoside, Glycerin,
    Acrylates Crosspolymer-4, PEG-120 Methyl Glucose Dioleate, Sodium Hydroxide, Carica Papaya (Papaya) Fruit Extract, Psidium Guajava (Guava) Fruit Extract, Panthenol, Synthetic Wax, Fragrance

  • QUESTIONS

    Questions or comments?
    Call 1-305-622-7474 Mon-Fri 9 am-5 pm

  • PACKAGE LABEL

    NDC 74553-016-01

    Facial Scrub

  • INGREDIENTS AND APPEARANCE
    OKAY FACIAL SCRUB 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74553-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    Glycerin (UNII: PDC6A3C0OX)  
    ACRYLATES CROSSPOLYMER-4 (UNII: GEV2EL4D9G)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PAPAYA (UNII: KU94FIY6JB)  
    GUAVA (UNII: 74O70D6VG0)  
    Panthenol (UNII: WV9CM0O67Z)  
    SYNTHETIC WAX (1800 MW) (UNII: 248P1AUJ90)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74553-016-01170 g in 1 TUBE; Type 0: Not a Combination Product09/11/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/11/2023
    Labeler - Xtreme Tools International, Inc (125398904)
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