Label: ALA-SEPTIC- salicylic acid lotion

  • NDC Code(s): 59434-134-00
  • Packager: Ala-Septic Pharmaceutical Research LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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  • Drug Facts

  • Active Ingredients

    Salicylic Acid 2.00%

    Purpose

    Seborrheic Dermatitis, Psoriasis

  • Use For:

    For relief of the symptoms of seborrheic dermatitis and psoriasis.

  • Warning:

    • For external use only.

    When using this product

    • Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

    Ask a doctor before using this product if

    • condition covers a large area of the body

    Stop use and ask a doctor if

    • condition worsens or does not improve after regular use of this product as directed.

    Keep out of reach of children.

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

    If pregnant or breast-feeding,

    ask a health professional before use

  • Directions:

    • Apply to affected areas one to four times daily or as directed by a doctor.
  • Other Ingredients:

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Benzoic Acid, Butylene Glycol, C13-14 Isoparaffin, Ethylhexylglycerin, Glycyrrhiza Glabra (Licorice) Root Extract, Iodoquinol, Isopropyl Myristate, Larrea Tridentata Extract, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Phenoxyethanol, Polyacrylamide, Polysorbate-20, SD-Alcohol 40B, Tocopheryl Acetate (Vitamin-E).

  • Package Labeling:

    BottleLabel

  • INGREDIENTS AND APPEARANCE
    ALA-SEPTIC 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59434-134
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    IODOQUINOL (UNII: 63W7IE88K8)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    LARREA TRIDENTATA LEAF (UNII: PK0TXD049P)  
    LAURETH-7 (UNII: Z95S6G8201)  
    MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59434-134-00113 g in 1 BOTTLE; Type 0: Not a Combination Product03/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03203/01/2021
    Labeler - Ala-Septic Pharmaceutical Research LLC (964652692)
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