Label: ST. IVES- acne control apricot scrub lotion

  • NDC Code(s): 64942-2081-1, 64942-2081-2
  • Packager: CONOPCO Inc. d/b/a Unilever
  • 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 August 4, 2022

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  • ST. IVES ACNE CONTROL APRICOT SCRUB - (Salicylic Acid) lotion

  • Active ingredient


    Salicylic Acid (2%)

  • Purpose


    Acne Treatment

  • Uses

    For the managemnet of acne
    Helps keep skin clear of new blackheads and acne blemishes

  • 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 occues, only use one topical acne medication at a time.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    Squeeze scrub onto fingertips and gently massage onto damp skin. Spread in small circular motions, then rinse and glow! For best results, use 2-3 times a week

  • Inactive ingredients

    Water (Aqua), Juglans Regia (Walnut) Shell Powder, Glyceryl Stearate SE, Glycerin, Cetyl Alcohol, Zea Mays (Corn) Kernel Meal, Cetearyl Alcohol, Triethanolamine, Cocamidopropyl Betaine, PEG-100 Stearate, Glyceryl Stearate, Carbomer, Ceteareth-20, Prunus Armeniaca (Apricot) Seed Powder, Prunus Armeniaca (Apricot) Fruit Extract, Sodium Methyl Lauroyl Taurate, Fragrance (Parfum), Polysorbate 60, Disodium EDTA, Iodopropynyl Butylcarbamate, Phenoxyethanol, Limonene, Linalool, Titanium Dioxide (CI 77891).

  • Questions or comments?

    USA: 1-866-912-9867

  • Packaging

    St. Ives Acne Apricot Scrub

  • INGREDIENTS AND APPEARANCE
    ST. IVES 
    acne control apricot scrub lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2081
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.02 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAUROYL METHYL TAURATE (UNII: H5K9S87SP3)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CORN GRAIN (UNII: C1Z9U7094Z)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    APRICOT (UNII: 269CJD5GZ9)  
    PRUNUS ARMENIACA SEED (UNII: 75356789IW)  
    JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2081-1170 g in 1 TUBE; Type 0: Not a Combination Product08/04/2022
    2NDC:64942-2081-2255 g in 1 TUBE; Type 0: Not a Combination Product08/04/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D08/04/2022
    Labeler - CONOPCO Inc. d/b/a Unilever (001375088)
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