Label: PEACH SLICES 3 STEP ACNE STARTER KIT- salicylic acid kit

  • NDC Code(s): 81515-540-00, 81515-541-01, 81515-542-01, 81515-543-01
  • Packager: Peach & Lily, Inc
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated August 14, 2024

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  • Drug Facts:

  • Active ingredient 

    Salicylic Acid 2%

    Purpose

    Acne medication

  • Use:

    For the treatment of acne

  • Warnings:

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

    Sun Alert:

    Because this product may make your skin more sensitive to the sun, be certain you have adequate sunscreen protection while using this product and for a week after you discontinue use.

    Keep out of reach of children.

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

  • Directions:

    • Wet face.
    • Dispense product into hands and massage gently onto face and neck, avoiding the delicate eye area.
    • Cover the entire affected area with a thin layer and rinse thoroughly with warm water 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), Glycerin, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Betaine, Sodium Chloride, Cucumis Sativus (Cucumber) Fruit Water, Sodium Hyaluronate, Centella Asiatica Extract, Malpighia Emarginata (Acerola) Fruit Extract, Sodium Benzoate, Butylene Glycol, Potassium Sorbate, Caprylyl Glycol, 1,2-Hexanediol, Sodium Hydroxide, Citric Acid, Ethylhexylglycerin, Phenoxyethanol

  • Questions or Comments?

    1-866-519-4752

  • Drug Facts:

  • Active ingredient

    Salicylic Acid 2%

    Purpose

    Acne medication

  • Use:

    For the treatment of acne

  • Warnings:

    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 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.

    Sunburn Alert:

    • This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn.
    • Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterward.

    Keep out of reach of children.

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

  • Directions:

    • Cleanse 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), Butylene Glycol, Arginine, Allantoin, Cucumis Sativus (Cucumber) Fruit Water, Glycerin, Centella Asiatica Extract, Malpighia Emarginata (Acerola) Fruit Extract, Lactic Acid, Glycolic Acid, Potassium Sorbate, Sodium Benzoate, Citric Acid

  • Questions or Comments?

    1-866-519-4752

  • Drug Facts:

  • Active ingredient

    Salicylic Acid 0.5%

    Purpose

    Acne medication

  • Use:

    For the treatment of acne

  • Warnings:

    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 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

    Sun Alert:

    Because this product may make your skin more sensitive to the sun, be certain you have adequate sunscreen protection while using this product and for a week after you discontinue use.

    Keep out of reach of children.

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

  • Directions:

    • Cleanse 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), Caprylic/Capric Triglyceride, Propanediol, Butylene Glycol, Cetyl Ethylhexanoate, Ethoxydiglycol, Glyceryl Stearate, 1,2-Hexanediol, Cetearyl Alcohol, Cucumis Sativus (Cucumber) Fruit Water, Centella Asiatica Extract, Sodium Acetylated Hyaluronate, Sodium Hydrolyzed Crosspolymer, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate, Sclerotium Gum, Malpighia Emarginata (Acerola) Fruit Extract, Glycerin, Allantoin, Sodium Benzoate, Potassium Sorbate, Potassium Hydroxide, Sodium Phytate, Niacinamide, Polyacrylate Crosspolymer-6, Citric Acid, Ethylhexylglycerin, T-Butyl Alcohol, Pentylene GLycol, Sodium Polyacrylate

  • Questions or Comments?

    1-866-519-4752

  • Package Labelling: Kit (81515-540-00)

    Kit.jpg

  • Package Labelling: 81515-541-01

    Acne Clarifying.jpgAcne Clarifying2.jpg

  • Package Labelling: 81515-542-01

    Acne Exfoliating.jpg

  • Package Labelling: 81515-543-01

    Acne Oil.jpgAcne Oil2.jpg

  • INGREDIENTS AND APPEARANCE
    PEACH SLICES 3 STEP ACNE STARTER KIT 
    salicylic acid kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81515-540
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81515-540-001 in 1 KIT08/14/2024
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 TUBE 30 mL
    Part 21 BOTTLE 30 mL
    Part 31 TUBE 30 mL
    Part 1 of 3
    ACNE CLARIFYING CLEANSER SALICYLIC ACID ACNE TREATMENT SULFATE FREE 
    salicylic acid gel
    Product Information
    Item Code (Source)NDC:81515-541
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    BETAINE (UNII: 3SCV180C9W)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CUCUMBER FRUIT OIL (UNII: R81Y52NPCT)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    ACEROLA (UNII: XDD2WEC9L5)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81515-541-011 in 1 CARTON
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/14/2024
    Part 2 of 3
    ACNE EXFOLIATING TONER SALICYLIC ACID ACNE TREATMENT ALCOHOL FREE 
    salicylic acid solution
    Product Information
    Item Code (Source)NDC:81515-542
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ARGININE (UNII: 94ZLA3W45F)  
    ALLANTOIN (UNII: 344S277G0Z)  
    CUCUMBER FRUIT OIL (UNII: R81Y52NPCT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    ACEROLA (UNII: XDD2WEC9L5)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81515-542-011 in 1 CARTON
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/14/2024
    Part 3 of 3
    ACNE OIL FREE MOISTURIZER SALICYLIC ACID ACNE TREATMENT SILICONE FREE 
    salicylic acid cream
    Product Information
    Item Code (Source)NDC:81515-543
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CETYL ETHYLHEXANOATE (UNII: 134647WMX4)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CUCUMBER FRUIT OIL (UNII: R81Y52NPCT)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    BETASIZOFIRAN (UNII: 2X51AD1X3T)  
    ACEROLA (UNII: XDD2WEC9L5)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALLANTOIN (UNII: 344S277G0Z)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PHYTATE SODIUM (UNII: 88496G1ERL)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81515-543-011 in 1 CARTON
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/14/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/14/2024
    Labeler - Peach & Lily, Inc (079906552)
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