Label: IT COSMETICS BYE BYE BREAKOUT CONCENTRATED DERMA SERUM ACNE TREATMENT- salicylic acid lotion

  • NDC Code(s): 49967-026-01, 49967-026-02, 49967-026-03
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 28, 2023

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  • Active ingredient


    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Use

    • for the treatment of acne
    • helps prevent new acne blemishes from forming
  • 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. 

  • 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 ingrease to two or three times dialy if neded or as directed by a doctor
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other dayl
  • Inactive ingredients

    water, glycerin, niacinamide, lactic acid, sodium hydroxide, zinc PCA, aloe barbadensis leaf juice, butylene glycol, chlorphenesin, sodium hyaluronate, trisodium ethylenediamine disuccinate, alteromonas ferment extract, citric acid, potassium sorbate, sodium benzoate

  • Questions or comments?

    Call 800-620-3950

  • PRINCIPAL DISPLAY PANEL

    image of a carton

    image of a carton
  • INGREDIENTS AND APPEARANCE
    IT COSMETICS BYE BYE BREAKOUT CONCENTRATED DERMA SERUM ACNE TREATMENT 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-026
    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)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ZINC PIDOLATE (UNII: C32PQ86DH4)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    ALTEROMONAS MACLEODII POLYSACCHARIDES (UNII: AP6XG2GR8Z)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-026-011 in 1 CARTON04/01/2022
    130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:49967-026-024 mL in 1 PACKET; Type 0: Not a Combination Product04/01/202204/01/2022
    3NDC:49967-026-034 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00604/01/2022
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-026) , pack(49967-026)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dimensional Merchandising Inc.076693183pack(49967-026)
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