Label: DERMACLEAR PADS- salicylic acid liquid

  • NDC Code(s): 62742-4076-1, 62742-4076-2
  • Packager: Allure Labs
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 5, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient - Salicylic Acid 2%

  • PURPOSE

    Purpose: Acne Treatment

  • INDICATIONS & USAGE

    Uses: For treatment of Acne

  • WARNINGS

    Warnings:

    • For external use only.
    • Overuse of this product will cause dryness.
  • DO NOT USE

    Do not use if you have sensitive skin.

  • WHEN USING

    When using this product:

    • Avoid contact with the eyes, lips and mouth.
    • 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.
    • If sensitive to the sun or when increased sun exposure is expected, use a sunscreen.
  • STOP USE

    Stop use and ask a doctor:

    • If severe skin irritation occurs.
    • When using other topical medication at the same time.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children:

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

    Gently rub pad over any area in need. Use every other night or as recommended by your skin care prifessional. Keep the lid securely closed to prevent evapration. To avoid dryness, do not overuse. Not recommended for those with aspirin / NASID allergies.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Alcohol Denat., Water (Aqua), Glycerin, PEG-8/SMDI Copolymer, Glycolic Acid, Aloe Barbadensis Leaf Juice, Ammonium Hydroxide, Melaleuca Alternifolia Leaf Oil, Allantoin, Limonene.

  • PRINCIPAL DISPLAY PANEL

    Manufactured for DermaQuest®, Inc.

    Hayward, CA 94544

    1272 GK, NL Made in USA

    dermaquestinc.com

    IMGDERMPADS

  • INGREDIENTS AND APPEARANCE
    DERMACLEAR PADS 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4076
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    AMMONIA (UNII: 5138Q19F1X)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4076-21 in 1 CARTON05/08/2015
    1NDC:62742-4076-185 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00605/08/2015
    Labeler - Allure Labs (926831603)
    Registrant - Allure Labs (926831603)
    Establishment
    NameAddressID/FEIBusiness Operations
    Allure Labs926831603manufacture(62742-4076)
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