Label: TRIPLE X-LOTION- glycolic acid, sulfur, salicylic acid lotion

  • NDC Code(s): 80724-201-01, 80724-201-02
  • Packager: EMS TRADE
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 12, 2023

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

  • Active ingredient[s]

    Glycolic Acid 3%

    Sulfur 3%

    Salicylic Acid 0.5%

  • Purpose

    Acne treatment

  • Use[s]

    The Serum to relive irritation of troubled skin, especially for sensitive skin type (Hypoallergenic test completed)

    The Lotion to relive and eliminate sebum and dead keratin cells inside the pores, the root cause of acne skin. (Suitable for acne-prone skin type)

  • Warnings

    For external use only.

    Do not use on damaged or broken skin.

    When using this product keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • Stop use and ask a doctor

    if irritation occurs.

  • Keep out of reach of children

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

  • Directions

    *Before use this product, please read the directions and warnings carefully

    *The Lotion should be used at night time (The Serum is recommended to use in the morning and night time)

    • STEP1 Serum After washing a face and apply toner first then absorbing the Serum to entire face at morning and night time.
    • STEP2 Lotion After using Serum (STEP1), absorbing the Lotion to entire face except around eyes and lips areas at night time only.
  • Inactive ingredients

    • Triple X Serum Water, Butylene Glycol , Portulaca Oleracea Extract, Sodium Hyaluronate, Hexacarboxymethyl Dipeptide-12, Propandiol, Sodium Polyglutamate, Dryopteris Crassirhizoma Extract, Forsythia Suspensa Fruit Extract, Centella Asiatica Extract, Aloe Barbadensis Leaf Juice Powder, Sophora Flavescens Root Extract, Paeonia Suffruticosa Root Extract, Scutellaria Baicalensis Root Extract , Zanthoxylum Piperitum Fruit Extract, Beta-Glucan¸ Betaine, Dipotassium Glycyrrhizate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Syringa Vulgaris (Lilac) Leaf Cell Culture Extract , 1,2-Hexanediol, Sodium Hydroxide
    • Triple X Lotion Water, Cyclopentasiloxane, Butylene Glycol , PPG-15 Stearyl Ether, Dimethicone, Steareth-2, Cetyl Alcohol, Steareth-21, Panthenol , Dipentaerythrityl Hexa C5-9 Acid Esters, Hexacarboxymethyl Dipeptide-12, Glycerin, Stearic Acid, Centella Asiatica Extract, Achillea Millefolium Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Brassica Oleracea Italica (Broccoli) Sprout Extract, Squalane, Dextrin Palmitate, Sodium Polyglutamate, Zanthoxylum Piperitum Fruit Extract, Paeonia Suffruticosa Root Extract, Scutellaria Baicalensis Root Extract , Sophora Flavescens Root Extract, Syringa Vulgaris (Lilac) Leaf Cell Culture Extract , Tocopheryl Acetate, sh-Oligopeptide-1, rh-Polypeptide-1, rh-Polypeptide-1, Copper Tripeptide-1, Nicotinoyl Hexapeptide-44, sh-Octapeptide-4, 1,2-Hexanediol, Lecithin, Houttuynia Cordata Extract, Chamomilla Recutita (Matricaria) Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Dipotassium Glycyrrhizate, Polysorbate 20, Capryloyl Glycine, Rosmarinus Officinalis (Rosemary) Leaf Oil, Xanthan Gum, Sodium Hyaluronate, Sodium Hyaluronate, Sodium Hydroxide, Sorbitol, Disodium EDTA
  • Package Label

    30ml NDC: 80724-201-01 Label

    60ml NDC: 80724-201-02 Label

  • INGREDIENTS AND APPEARANCE
    TRIPLE X-LOTION 
    glycolic acid, sulfur, salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80724-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.5 g  in 100 mL
    GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID3 g  in 100 mL
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    DIPENTAERYTHRITYL HEXA C5-9 ACID ESTERS (UNII: D818OLQ51Z)  
    BROCCOLI SPROUT (UNII: 128UH9LOAE)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    NEPIDERMIN (UNII: TZK30RF92W)  
    BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    CHAMOMILE (UNII: FGL3685T2X)  
    STEARETH-2 (UNII: V56DFE46J5)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    PREZATIDE COPPER (UNII: 6BJQ43T1I9)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
    STEARETH-21 (UNII: 53J3F32P58)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)  
    PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)  
    SQUALANE (UNII: GW89575KF9)  
    DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)  
    ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK)  
    HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SORBITOL (UNII: 506T60A25R)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80724-201-0130 mL in 1 TUBE; Type 0: Not a Combination Product10/15/2020
    2NDC:80724-201-0260 mL in 1 TUBE; Type 0: Not a Combination Product10/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/15/2020
    Labeler - EMS TRADE (689944382)
    Registrant - EMS TRADE (689944382)
    Establishment
    NameAddressID/FEIBusiness Operations
    EMS TRADE689944382manufacture(80724-201)