Label: B-LUCID TARGETED BODY ACNE GEL- salicylic acid gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 1, 2023

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

  • Drug Facts

  • Active Ingredient

    Salicylic Acid 2%

    Purpose

    Acne treatment

  • Uses

    • For the treatment of acne

  • Warnings

    For external use only.

    Keep out of reach of children.

    • 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. • Do not get into eyes. tt excessive skin irritation develops or increases, discontinue use and consult a doctor. • If product is swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply a thin layer directly to acne on the chest, booty, and other affected areas. • Massage into the skin in circular motions until fully absorbed. • Use twice a day for best results.

  • Inactive Ingredients:

    Water, Glycerin, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Propanediol, Caprylic/Capric Triglyceride, C12-C15 Alkyl Benzoate, Isostearyl Linoleate, PEG-100 Stearate, Glyceryl Stearate, Niacinamide, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Glycolic Acid, Epilobium Fleischeri Flower/Leaf/Stem Extract, Zinc PCA, Centella Asiatica Extract, Camellia Sinensis Leaf Extract, Tocopherol, Polyglyceryl-4 Caprate, Silica, Amylopectin, Sorbitan Isostearate, Parfum (Fragrance), Ethylhexylglycerin, Polydextrose, Dextrin, Phenoxyethanol, Citric Acid, Sodium Hydroxide, Coumarin, CI 42090 (Blue 1).

  • Other Information

    Protect this product from excessive heat and direct sun.

  • Question or Comments:

    1-800-253-1983

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    B-LUCID TARGETED BODY ACNE GEL 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83010-010
    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)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ISOSTEARYL LINOLEATE (UNII: 4778M3HR0N)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    ZINC PIDOLATE (UNII: C32PQ86DH4)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYDEXTROSE (UNII: VH2XOU12IE)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    COUMARIN (UNII: A4VZ22K1WT)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83010-010-001 in 1 CARTON01/01/2023
    1100 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00601/01/2023
    Labeler - Maelys Cosmetics, LTD (532018258)