Label: SKIN LAUNDRY. CLEAN SLATE EXFOLIATING 2 SALICYLIC ACID TREATMENT GEL CLEANSER CLEANSE EXFOLIATE- salicylic acid gel

  • NDC Code(s): 83727-294-00
  • Packager: Skin Laundry Holdings, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 6, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

  • Active ingredient

    Salicylic Acid 2%

    Purpose

    Acne treatment

  • Uses

    ● For the treatment of acne.

  • Warnings

    For external use only.

    When using this product

    • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. 
    • Avoid contact with eyes. If contact occurs, flush thoroughly with water. 

    Keep out of the reach of children.

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

    Stop and ask a doctor:

    if skin irritation occurs or gets worse

  • Directions

    • Use twice daily 
    • Wet face, then work product into a lather 
    • Massage onto face avoiding the eyes
    • Rinse thoroughly 
    • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  • Other Information

    • Protect the product in this container from excessive heat and direct sun.
  • Inactive Ingredients

    Water (Aqua), Glycerin, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Betaine, Sodium Chloride, 1,2-hexanediol, Caprylyl Glycol, Sodium Hydroxide, Sodium Hyaluronate, Centelia Asiatica Extract

  • Questions or Comments?

    Product questions, email Hello@skinlaundry,com

    You may report side effects to FDA at 1-800-FDA-1088

  • Package Labeling:

    Package

  • INGREDIENTS AND APPEARANCE
    SKIN LAUNDRY. CLEAN SLATE EXFOLIATING 2 SALICYLIC ACID TREATMENT GEL CLEANSER CLEANSE EXFOLIATE 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83727-294
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    BETAINE (UNII: 3SCV180C9W)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83727-294-00150 mL in 1 BOTTLE; Type 0: Not a Combination Product10/14/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00610/14/2023
    Labeler - Skin Laundry Holdings, Inc. (118584348)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!