Label: AGE BRIGHT CLEARING SERUM- salicylic acid liquid

  • NDC Code(s): 68479-184-00, 68479-184-01, 68479-184-02
  • Packager: Dermalogica, Inc
  • 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 June 30, 2022

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Salicylic Acid (2.0%)

  • Purpose

    Acne treatment

  • Indications

    For the treatment of acne

  • Warnings

    For external use only

    When using this product

    • Skin irritation and dryness are 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.

    Keep out of reach of children.

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

    • Apply a thin layer and allow to dry. Use all over the face and under your recommended Dermalogica Moisturizer twice a day, as needed.
    • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  • Inactive Ingredients

    Water/Aqua/Eau, Niacinamide, Butylene Glycol, PEG-40 Hydrogenated Castor Oil, Lentinus Edodes Mycelium Extract, Glyceryl Glucoside, Salvia Sclarea (Clary) Oil, Phytic Acid, Terpineol, Thymol, Citrus Aurantium Dulcis (Orange) Peel Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Lavandula Hybrida Oil, Pelargonium Graveolens Flower Oil, Lavandula Angustifolia (Lavender) Oil, Citrus Limon (Lemon) Peel Oil, Polydextrose, Glycerin, Dextrin, Amylopectin, Caprylyl Glycol, Ethylhexylglycerin, Xanthan Gum, Pentylene Glycol, Sodium Hydroxide, Isoamyl Laurate, Phenoxyethanol.

  • Questions or comments

    Call toll free

    1-800-831-5150 in the US.

  • PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton

    NEW

    Active Clearing

    1 US FL OZ / 30 mL e

    PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton
  • INGREDIENTS AND APPEARANCE
    AGE BRIGHT CLEARING SERUM 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68479-184
    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)  
    Niacinamide (UNII: 25X51I8RD4)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    LENTINULA EDODES MYCELIUM (UNII: CU2S39TB8O)  
    CLARY SAGE OIL (UNII: 87L0D4U3M0)  
    FYTIC ACID (UNII: 7IGF0S7R8I)  
    Terpineol (UNII: R53Q4ZWC99)  
    Thymol (UNII: 3J50XA376E)  
    ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    LAVANDIN OIL (UNII: 9RES347CKG)  
    Pelargonium Graveolens Flower Oil (UNII: 3K0J1S7QGC)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    LEMON OIL, COLD PRESSED (UNII: I9GRO824LL)  
    Polydextrose (UNII: VH2XOU12IE)  
    Glycerin (UNII: PDC6A3C0OX)  
    DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
    AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777)  
    Caprylyl Glycol (UNII: 00YIU5438U)  
    Ethylhexylglycerin (UNII: 147D247K3P)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Pentylene Glycol (UNII: 50C1307PZG)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Isoamyl Laurate (UNII: M1SLX00M3M)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68479-184-021 in 1 CARTON06/06/2019
    130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:68479-184-003 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/06/2019
    3NDC:68479-184-0110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/06/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart333D06/06/2019
    Labeler - Dermalogica, Inc (177698560)
    Establishment
    NameAddressID/FEIBusiness Operations
    McKenna Labs, Inc.090631412MANUFACTURE(68479-184)
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!