Label: CLEAR ACNE SPOT TREATMENT- acne spot treatment liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 7, 2024

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

  • Drug Facts

    Active Ingredient

    Salicylic Acid 2.0%

    Purpose

    Acne Treatment

    Use

    • For the treatment of acne

    Warnings

    For external use only

    When using this product

    • avoid unnecessary sun exposure and use sunscreen
    • avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water
    • using other topical acne medication at the same time or immediately following the use of this product may increase dryness or irritation of the skin. If this occurs, only one medication at a time should be used, unless otherwise directed by a doctor

    Stop use and ask a doctor

    • if irritation persists

    Keep out of reach of children

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

    Directions

    • cleanse the skin thoroughly before applying medication
    • cover the entire affected area with a thin layer 1 to 3 times daily
    • because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 times daily if needed or as directed by a doctor
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other day
    • for children under 10 years of age and under, consult your physician

    Inactive Ingredients

    acrylates/C10-30 alkyl acrylate crosspolymer, alcohol, amur cork tree (Phellodendron amurense) bark extract, baikal skullcap (Scutellaria baicalensis) root extract, benzyl alcohol, capryloyl glycine, Chinese rhubarb (Rheum palmatum) root extract, chlorphenesin, chrysanthemum (Chrysanthemum indicum) flower extract, cinnamon (Cinnamomum zeylanicum) bark extract, common purslane (Portulaca oleracea) extract, fragrance, glycerin, great burnet (Sanguisorba officinalis) root extract, hexylene glycol, Norway spruce (Picea abis) extract, propanediol, sarcosine, SD Alcohol 40-C, sodium phytate, tromethamine, water, xanthan gum

    Questions or Comments?

    1-855-626-6606

  • SPL UNCLASSIFIED SECTION

    Made in USA
    (US and non-US ingredients)
    Manufactured for Kamedis
    Paterson, NJ 07503
    1-855-626-6606

    www.kamedisUSA.com

  • Carton label

    image description

  • INGREDIENTS AND APPEARANCE
    CLEAR ACNE SPOT TREATMENT 
    acne spot treatment liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50718-0032
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID28.8 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)  
    ALCOHOL (UNII: 3K9958V90M)  
    PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)  
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)  
    PURSLANE (UNII: M6S840WXG5)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    RHEUM PALMATUM ROOT (UNII: G025DAL7CE)  
    SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    PICEA ABIES WOOD (UNII: 72GZ8K8996)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SARCOSINE (UNII: Z711V88R5F)  
    HEXASODIUM PHYTATE (UNII: ZBX50UG81V)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50718-0032-11 in 1 CARTON01/01/2018
    122 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00601/01/2018
    Labeler - Kamedis (080311300)
    Establishment
    NameAddressID/FEIBusiness Operations
    Biogenesis Inc.069117328manufacture(50718-0032)