Label: RE-FRESH SCALP CARE- salicylic acid shampoo

  • 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 December 7, 2022

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  • RE-FRESH SCALP CARE HONEYSUCKLE + CLEANSE ANTI-DANDRUFF SHAMPOO - salicylic acid liquid

    RE-fresh Scalp Care Honeysuckle + Cleanse Anti-Dandruff Shampoo

  • Drug Facts

    Active ingredientSalicylic Acid (2.0%)

  • Purpose

    Anti-dandruff

  • Use

    Helps prevent and control recurrence of itching, flaking and irritation associated with dandruff.

  • Warnings

    For external use only

    When using this product Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

    Stop use and ask a doctor if Condition worsens or does not improve after regular use of this product as directed.

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Inactive Ingredients

    Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Glycerin, Lonicera Japonica (Honeysuckle) Flower Extract, Salix Alba (Willow) Bark Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Arctium Lappa Root Extract, Ginkgo Biloba Leaf Extract, Salvia Officinalis (Sage) Leaf Extract, Hippophae Rhamnoides Fruit Extract, Citric Acid, Fragrance (Parfum), Sodium Benzoate, Polyquaternium-10, Disodium EDTA, Alpha-Isomethyl Ionone, Hexyl Cinnamal, Linalool.

  • Directions

    For best results use at least twice per week or as directed by a doctor. Massage into scalp and hair. Rinse.

  • Questions/comments?

    Call toll-free 1-800-671-3998

  • Packaging

    RefreshHoneysuckleAntiDandruffSH

  • INGREDIENTS AND APPEARANCE
    RE-FRESH SCALP CARE 
    salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1641
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
    GINKGO (UNII: 19FUJ2C58T)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1641-1400 mL in 1 CONTAINER; Type 0: Not a Combination Product05/10/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H10/19/2018
    Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)
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