Label: ANTI-EVERYTHING FACE SERUM- salicylic acid serum liquid

  • NDC Code(s): 54111-180-01
  • Packager: Bentley laboratories, llC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 5, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Drug Facts

    Active Ingredients

    Salicylic Acid  2.0%

  • PURPOSE

    Purpose

    Acne Treatment

  • INDICATIONS & USAGE

    Uses
    • For tha treatment of acne
    • Reduces tha number of aena pimples,
    blackheads, whiteheads and allows
    skin to heal
    • Pllnatrates paras to clear I110lIl acne
    blemishes
    • Helps prevent new acne blemishes
    lromformlng

  • WARNINGS

    Warnings
    For external use only

    Do not use if you have very sensitive
    skin or known allergy to aspirin

    Slop use and ask a doctor if
    excessive itching, dryness, redness,
    burning, or swelling occurs or if these
    symptoms persist

    When ullng this product • Keep
    away from eyes, lips, and other
    mucous membranes. If contact occurs,
    flush thoroughly with water.• Using
    other topical acne medications at the
    same time or immediately following
    use of this product may increase
    dryness or irritation of the skin. If this
    occurs, only one medication should be
    used unless directed by doctor.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children. If
    swallowed get medical help or contact
    Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions
    • Squeeze 1-2 pumps on to fingertlps.
    Apply a thin layer to clean,
    dry skin in the morning. Avoid eye
    area. Suggested use In AM.

    • At first, use every other day. Then
    up to twice a day as tolerated
    • Use sunscreen during the day while
    using this product
    • Because excessive drying of the skin
    may occur, start with one application
    daily, then gradually increase if needed
    or as directed by a doctor.
    • If bothersome dryness or peeling
    occurs, reduce the application.
    • Store dry at room temperature

  • INACTIVE INGREDIENT

    Inactive ingredients Water,
    Glycolic Acid, Isopentyldiol, Glycerin,
    HDI/Trimethylol Hexyllactone
    Crosspolymer, Cetearyl Alcohol,
    Ammonium Acryloyldimethyltaurate/VP
    Copolymer, Sodium Hydroxide, Tapioca
    Starch, C13-15 Alkane, Phenoxyethanol,
    1,2-Hexanediol, Panthenol, Eucalyptus
    Globulus Leaf Oil, Tetrasodium Glutamate
    Diacetate, Cladonia Stellaris Extract,
    Silica, Sodium Hyaluronate, Iron Oxides
    (CI 77492), Ricinus Communis (Castor)
    Seed Oil, Niacinamide,
    Chlorophyllin-Copper Complex, Limonene

  • SPL UNCLASSIFIED SECTION

    Other Information 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 afterwards.

  • QUESTIONS

    Questions or comments?

    Email us at HI@oarsandalps.com

  • Product Packaging: OARS + ALPS ANTI-EVERYTHING FACE SERUM

    OARS + ALPS

    ANTI-EVERYTHING

    FACE SERUM

    2% SALICYLIC ACID

    5% GLYCOLIC ACID

    1 Fl. Oz. / 20 mL

    Manufactured for

    Oars + Alps LLC

    Chicago, IL 60661

    O-A Serum Cartn

    O A 1oz Serum Botl

    res 080624

  • INGREDIENTS AND APPEARANCE
    ANTI-EVERYTHING FACE SERUM 
    salicylic acid serum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54111-180
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid2.0 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    ISOPENTYLDIOL (UNII: 19NOL5474Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    C13-15 ALKANE (UNII: 114P5I43UJ)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
    CLADONIA CRISTATELLA WHOLE (UNII: YWE2XUB3DS)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    SODIUM COPPER CHLOROPHYLLIN (UNII: 1D276TYV9O)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54111-180-011 in 1 CARTON08/08/2024
    130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/08/2024
    Labeler - Bentley laboratories, llC (068351753)