Label: PHARMA CLEAR CLEANSER- salicylic acid gel

  • NDC Code(s): 67879-101-11
  • Packager: PHARMAGEL INTERNATIONAL INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 7, 2024

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  • ACTIVE INGREDIENTS

    Salicylic Acid 2.0%

  • PURPOSE

    Acne Medication

  • USES:

    Use for treatment of acne and to decrease bacteria on the skin.

  • WARNINGS

    For external use only

  • When using this product:

    • avoid contact with the eyes. If product gets into the eyes, rinse thoroughly with water.

    • Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the 

       skin. If this occurs, only one medication should be used unless directed by a doctor.

    • Limit use to the face and neck.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DIRECTIONS:

    Wet area. Dispense product into hands and massage gently onto face and body, avoiding the eye area. Rinse thoroughly with warm water and pat dry. For best results, use twice daily.

  • INACTIVE INGREDIENTS:

    WATER (AQUA), SODIUM C14-16 OLEFIN SULFONATE, ACRYLATES COPOLYMER, COCAMIDOPROPYL BETAINE, GLYCERIN, CITRIC ACID, DISODIUM EDTA-COPPER, SODIUM HYDROXIDE, TRICLOSAN, PANTHENOL, BISABOLOL, GARCINIA MANGOSTANA (MANGOSTEEN) FRUIT EXTRACT, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE

  • PRINCIPAL DISPLAY PANEL

    PHK_1A_RL-2_2

  • INGREDIENTS AND APPEARANCE
    PHARMA CLEAR CLEANSER 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67879-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    GARCINIA MANGOSTANA FRUIT (UNII: 832X5KK78Y)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67879-101-11175 mL in 1 TUBE; Type 0: Not a Combination Product06/15/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/18/2015
    Labeler - PHARMAGEL INTERNATIONAL INC (603215182)
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