Label: CLEAR ACNE FACE CLEANSER- acne face cleanser 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 1.0%

    Purpose

    Acne Treatment

    Use

    • For the treatment of acne

    Warnings

    For external use only

    When using this product

    • avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water
    • using other topical acne medications 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

    • Wet face. Apply cleanser to hands, add water and work into lather. Gently massage all over face avoiding eye area. Rinse thoroughly and pat dry. Good for daily use.
    • 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 doctor.

    Inactive Ingredients

    water, sodium methyl cocoyl taurate, cocamidopropyl betaine, sodium lauroyl methyl isethionate, sodium cocoyl apple amino acids, glycerin, salt (sodium chloride), cocamide MEA, glyceryl stearate SE, stearic acid, myristic acid, common purslane (Portulaca oleracea) extract, soapberry (Sapindus mukurossi) fruit extract, squalane, hydrolyzed jojoba esters, methyl glucose caprate/caprylate/oleate & propanediol, trisodium ethylenediamine disuccinate, vitamin E (tocopheryl acetate), xanthan gum, benzyl alcohol, lauroyl lysine, chlorphenesin, sodium hydroxide, fragrance

    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 FACE CLEANSER 
    acne face cleanser liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50718-0031
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID14.4 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    PURSLANE (UNII: M6S840WXG5)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SQUALANE (UNII: GW89575KF9)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    LAUROYL LYSINE (UNII: 113171Q70B)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SAPINDUS MUKOROSSI FRUIT (UNII: 66H9NW427Y)  
    SODIUM LAUROYL METHYL ISETHIONATE (UNII: II6VCD3S6R)  
    SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    SODIUM COCOYL APPLE AMINO ACIDS (UNII: EB3U1PA61T)  
    METHYL GLUCOSE (UNII: QCF122NF3R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50718-0031-11 in 1 CARTON01/01/2018
    1100 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(50718-0031)