Label: DAILY MEDS- salicylic acid lotion

  • NDC Code(s): 49825-100-10, 49825-100-20
  • Packager: Bioelements
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 9, 2024

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  • active ingredient

    salicylic acid 2%

  • purpose

    acne treatment

  • indications

    clears acne pimples

  • warnings

    for external use only.

    keep out of reach of children,

    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. when using this product apply only to areas with acne.

  • 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 times daily if needed or as directed by doctor. if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

  • inactive ingredients

    Water (Aqua, Eau), Propanediol, Glycolic Acid, Sodium Hydroxide, Lactic Acid, Niacinamide, Cetyl Hydroxyethylcellulose, Maltodextrin, Potassium Azeloyl Diglycinate, Sodium Benzoate, Glycerin, Potassium Sorbate, Syringa Vulgaris (Lilac) Extract, Hydrated Silica, Camellia Oleifera Leaf Extract, Origanum Vulgare Leaf Extract, Thymus Vulgaris (Thyme) Extract, Disodium Phosphate, Silica Dimethyl Silylate, Amylopectin, Dextrin, Polydextrose, Sodium Phosphate

  • questions?

    call 1.800.433.6650

    monday - friday 7:30am - 4:30 pm mst

  • Principal Display Panel – 30 mL Carton Label

    bioelements

    daily meds™

    acne clearing serum
    with medicinal beta +
    alpha hydroxy acids plus
    niacinamide to target
    lines, tone + dullness

    ACNE ACTIVIST

    30 mL / 1 fl oz

    Figure
  • INGREDIENTS AND APPEARANCE
    DAILY MEDS 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49825-100
    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)  
    Propanediol (UNII: 5965N8W85T)  
    Glycolic Acid (UNII: 0WT12SX38S)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Lactic Acid, Unspecified Form (UNII: 33X04XA5AT)  
    Niacinamide (UNII: 25X51I8RD4)  
    Cetyl Hydroxyethylcellulose (350000 MW) (UNII: T7SWE4S2TT)  
    Maltodextrin (UNII: 7CVR7L4A2D)  
    Potassium Azeloyl Diglycinate (UNII: N02RVN6NYP)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Glycerin (UNII: PDC6A3C0OX)  
    Potassium Sorbate (UNII: 1VPU26JZZ4)  
    Syringa Vulgaris Flower (UNII: 9V5O040S3W)  
    Hydrated Silica (UNII: Y6O7T4G8P9)  
    Camellia Oleifera Leaf (UNII: 5077EL0C60)  
    Oregano (UNII: 0E5AT8T16U)  
    Thyme (UNII: CW657OBU4N)  
    Sodium Phosphate, Dibasic, Anhydrous (UNII: 22ADO53M6F)  
    Silica Dimethyl Silylate (UNII: EU2PSP0G0W)  
    Amylopectin, Unspecified Source (UNII: 4XO4QFV777)  
    Dextrin, corn (UNII: VAD2K35XAJ)  
    Polydextrose (UNII: VH2XOU12IE)  
    Sodium Phosphate (UNII: SE337SVY37)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49825-100-101 in 1 CARTON09/01/2024
    1NDC:49825-100-2030 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/01/2024
    Labeler - Bioelements (174813923)
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