Label: BLEACKHEAD REMOVING MEDICATED SCRUB DAYLOGIC- salicylic acid 2.00% lotion

  • 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 May 22, 2018

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredient                                                 Purpose
    Salicylic acid 2%..................................................Acne Medication

  • PURPOSE

  • INDICATIONS & USAGE

    Uses For the treatment of acne and helps clear blackheads

  • WARNINGS

    Warnings
    For external use only
    When using this product and other topical acne medications at
    the same time or immediately following use of this product,
    dryness or irritation of the skin may be increased. If this occurs,
    only one medication should be used unless directed by a doctor

  • 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. Avoid contact with
    eyes. If contact occurs, flush thoroughly with water.

  • DOSAGE & ADMINISTRATION

    Directions • wet face • gently massage product all over face for 20-30 seconds, avoiding eye area • rinse thoroughly and
    pat dry • recommended for daily use

  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Cetyl Alcohol, PPG-15
    Stearyl Ether, Microcrystalline Wax, Jojoba Esters, Steareth-21,
    Polysorbate 60, Ferric Ferrocyanide, Xanthan Gum, Potassium
    Cetyl Phosphate, Fragrance, Menthyl Lactate.

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    BLEACKHEAD REMOVING MEDICATED SCRUB  DAYLOGIC
    salicylic acid 2.00% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-7798
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Cetyl Alcohol (UNII: 936JST6JCN)  
    PPG-15 Stearyl Ether (UNII: 1II18XLS1L)  
    Microcrystalline Wax (UNII: XOF597Q3KY)  
    HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)  
    Steareth-21 (UNII: 53J3F32P58)  
    Polysorbate 60 (UNII: CAL22UVI4M)  
    Ferric Ferrocyanide (UNII: TLE294X33A)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)  
    MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-7798-4141 g in 1 TUBE; Type 0: Not a Combination Product09/15/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D09/15/2016
    Labeler - Rite Aid (014578892)
    Registrant - Product Quest Mfg (927768135)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg927768135manufacture(11822-7798) , label(11822-7798)
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!