Label: ALMAY CLEAR COMPLEXION PRESSED POWDER- salicylic acid powder

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 22, 2019

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  • ACTIVE INGREDIENT

    Salicylic Acid 2.0%

  • Purpose

    Acne Treatment

  • Uses:

    •Helps clear and prevent blemishes

  • Warnings:

    For external use only.

    Skin irritation and dryness is likely to occur if you use antother topica; acne medication at the same time. If irritation occurs, use only one topical acne medication at a time.

    Avoid contact with eyes. If contact occurs, flush throughly with water.

  • Directions

    Clean skin thoroughly

    before applying this product • 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 appli -

    cation daily, then gradually increase to 2

    or 3 times daily if needed or as directed

    by doctor. • If bothersome dryness or

    peeling occurs, reduce application to once

    a day or every other day.

  • Inactive Ingredients

    TALC, MAGNESIUM STEARATE, ZEA MAYS (CORN) STARCH, C12-15 ALKYL BENZOATE, NYLON-12, KAOLIN, PHENYL TRIMETHICONE, PHENOXYETHANOL, HYDROLYZED VEGETABLE PROTEIN, HYDROGENATED LECITHIN, SPIRAEA ULMARIA EXTRACT, METHYLSALICYLATYL GLYCYRRHETINATE, SILICA, SODIUM HYALURONATE

  • DOSAGE & ADMINISTRATION

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

  • Principal Display Panel

    Almay Clear Complexion Pressed Powder

    .28 Oz/ 8.0 g Almay CC Powder

  • INGREDIENTS AND APPEARANCE
    ALMAY CLEAR COMPLEXION PRESSED POWDER 
    salicylic acid powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0311-0721
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.002 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    WATER (UNII: 059QF0KO0R)  
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TALC (UNII: 7SEV7J4R1U)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)  
    NYLON-12 (UNII: 446U8J075B)  
    KAOLIN (UNII: 24H4NWX5CO)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    MICA (UNII: V8A1AW0880)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0311-0721-808 g in 1 CONTAINER; Type 0: Not a Combination Product01/02/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H01/02/2019
    Labeler - Almay, Inc. (064988652)
    Establishment
    NameAddressID/FEIBusiness Operations
    REVLON, INC.809725570manufacture(0311-0721)
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