Label: ACNE FIGHTING SPOT WITH ALOE CLEAR- salicylic acid gel

  • NDC Code(s): 70412-411-06
  • Packager: Zhejiang Ayan Biotech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2023

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

View All Sections
  • Drug Facts

  • Active ingredients

    Salicylic Acid 1%

    Purpose

    Acne Treatment

  • Uses

    • For the treatment of acne
    • Helps prevent new acne blemishes
  • Warnings

    For external use only.

    When using this product

    • Keep out of eyes. Rinse with water to remove.
    • 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.

    Stop use and ask a doctor if

    • rash occurs.

    Keep out of reach of children.

  • 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.
  • Other Information

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

    Water (Aqua), Alcohol, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Extract, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Camphor, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Aloe Barbadensis Leaf Extract, Camellia Sinensis Leaf Extract, Sodium Benzoate

  • Questions or comments

    1-855-353-7320

  • Package Labeling:

    Outer PackageInner Package

  • INGREDIENTS AND APPEARANCE
    ACNE FIGHTING SPOT WITH ALOE CLEAR 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70412-411
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    LAURETH-7 (UNII: Z95S6G8201)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70412-411-061 in 1 BOX06/01/2018
    16 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/01/2018
    Labeler - Zhejiang Ayan Biotech Co.,Ltd. (544377996)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Ayan Biotech Co.,Ltd.544377996manufacture(70412-411)
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!