Label: CLEAR ACNE FACE MOISTURIZER- acne face moisturizer lotion

  • 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 one to three times daily.
    • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three 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, consult your physician.

    Inactive Ingredients

    Alcohol, Arachidyl Alcohol, Arachidyl Glucoside, Ascorbyl Tetraisopalmitate, Baikal Skullcap (Scutellaria Baicalensis) Root Extract, Behenyl Alcohol, Benzyl Alcohol, Capryloyl Glycine, Carbomer, Cetyl Alcohol, Chlorphenesin, Chinese Rhubarb (Rheum Palmatum) Root Extract, Chrysanthemum (Chrysanthemum Indicum) Flower Extract, Cinnamon (Cinnamomum Zeylanicum) Bark Extract, Common Purslane (Portulaca Oleracea) Extract, Dicaprylyl Carbonate, Fragrance, Glucose, Glycerin, Hexylene Glycol, Norway Spruce (Picea Abis) Extract, Phenethyl Alcohol, Plankton Extract, Propanediol, Sarcosine, SD Alcohol 40-C, Shea Butter (Butyrospermum Parkii), Sodium Hydroxide, Sodium Phytate, Squalane, Stearyl Alcohol, Water, Xanthan Gum.

    Questions or Comments?

    1-855-626-6606

  • SPL UNCLASSIFIED SECTION

    Made in USA
    Manufactured for Kamedis
    Pennsylvania, 18109
    1-855-626-6606

    www.kamedis-usa.com

  • Carton label

    image description

  • INGREDIENTS AND APPEARANCE
    CLEAR ACNE FACE MOISTURIZER 
    acne face moisturizer lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50718-0033
    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
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    ALCOHOL (UNII: 3K9958V90M)  
    ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
    ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PURSLANE (UNII: M6S840WXG5)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    RHEUM PALMATUM ROOT (UNII: G025DAL7CE)  
    CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    PICEA ABIES WOOD (UNII: 72GZ8K8996)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SARCOSINE (UNII: Z711V88R5F)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PHYTATE SODIUM (UNII: 88496G1ERL)  
    SQUALANE (UNII: GW89575KF9)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    NORI (UNII: 477TV3P5UX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50718-0033-11 in 1 CARTON01/01/2018
    150 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(50718-0033)