Label: KILLA ACNE EXTRA STRENGTH 2 PACK- salicylic acid patch

  • 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 August 30, 2023

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  • ACTIVE INGREDIENT

    Salicylic Acid 2%

  • ASK DOCTOR

    Ask a doctor if irritation become severe.

  • KEEP OUT OF REACH OF CHILDREN

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

  • PURPOSE

    Uses:

    • For the management of acne.
    • Penetrates pores to eliminate most blemishes.
  • INACTIVE INGREDIENT

    Sodium Hyaluronate, phytosphingosine HCl, Niacinamide, Oligopeptide-10, Glycolic Acid, Madecassoside, 4-Butylresorcinol

  • Uses

    • For the management of acne.
    • Penetrates pores to eliminate most blemishes.
  • Directions and How to Use

    How to open:

    1. To remove a patch, peel the front, top corner and pull towards the center.

    2. Inside, you'll find a white tab with a slit on one side. Tear along that seam to reveal the KILLA ACNE Extra Strength patch.

    How to use:

    1. Cleanse skin thoroughly before applying the product.

    2. Once dry, apply KILLA ACNE Extra Strength pimple patch onto zit.

    3. Leave on for 2+ hrs for microdarts to dissolve (for best results leave on overnight).

  • WARNINGS

    For external use only.

  • PRINCIPAL DISPLAY PANEL

    PDP

  • INGREDIENTS AND APPEARANCE
    KILLA ACNE EXTRA STRENGTH 2 PACK 
    salicylic acid patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81746-899
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.0125 mg  in 0.6216 mg
    Inactive Ingredients
    Ingredient NameStrength
    4-BUTYLRESORCINOL (UNII: 2IK4UQ3ZGA)  
    PHYTOSPHINGOSINE HYDROCHLORIDE (UNII: TT871XV7TU)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    OLIGOPEPTIDE-10 (UNII: Q46328TRNK)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    MADECASSOSIDE (UNII: CQ2F5O6YIY)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81746-899-001660 mg in 1 BOX; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)08/30/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM00605/26/2023
    Labeler - ZitSticka, Inc. (117778611)
    Establishment
    NameAddressID/FEIBusiness Operations
    Raphas695914964manufacture(81746-899)
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