Label: EQUATE PURIFYING CLEANSER- benzoyl peroxide liquid

  • 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 21, 2020

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

  • ACTIVE INGREDIENT

    Active ingredient

    Benzoyl Peroxide 2.5%

  • PURPOSE

    Purpose

    Acne treatment

  • INDICATIONS & USAGE

    Use for the management of acne

  • WARNINGS

    Warnings

    For external use only

    Do not use this medication if you have very sensitive skin or if you are sensitive to benzoyl peroxide

    Ask a doctor or pharmacist before use if you are using other topical acne medications at the same

    time or immediately following use of this product. This may increase dryness or irritation of the skin. If

    this occurs, only one medication should be used unless directed by a doctor.

    When using this product  -avoid contact with eyes. If contact occurs, rinse eyes thoroughly with

    water  -keep away from lips and mouth  -avoid unnecessary sun exposure and use a sunscreen.

    Stop use and ask a doctor if skin irritation occurs.

  • 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 (1-800-222-1222).

  • DOSAGE & ADMINISTRATION

    Directions  -use morning and night. Apply a small (dime-sized) amount to dampened skin and

    gently massage for 1 to 2 minutes  -rinse thoroughly with warm water  -pat dry

    -if bothersome dryness or peeling occurs, reduce application to once a day or every other day

    - if going outside, use a sunscreen

  • OTHER SAFETY INFORMATION

    Other information  -this product may bleach hair or dyed fabrics

    -avoid storing at extreme temperatures (below 40F and above 100F)

  • INACTIVE INGREDIENT

    Inactive ingredients  water, disodium PEG-12 dimethicone sulfosuccinate, glyceryl

    stearate, PEG-100 stearate, tridecyl stearate, neopentyl glycol dicaprylate/dicaprate, tridecyl

    trimelliate, magnesium aluminum silicate, sorbitol, dimethyl isosorbide, silica, mannitol, sucrose,

    zea mays (corn) starch, polyvinyl alcohol, cetyl esters, propylene glycol, chamomillacutita recutita

    (matricaria) flower extract, xanthan gum, sodium hyalaurante, sodium PCA, fragrance

  • QUESTIONS

    Questions?  1-888-287-1915

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    EQUATE PURIFYING CLEANSER 
    benzoyl peroxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-644
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE3 g  in 120 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DISODIUM LAURETH-12 SULFOSUCCINATE (UNII: F8I0R9Q3ZX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    TRIDECYL STEARATE (UNII: A8OE252M6L)  
    NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)  
    TRIDECYL TRIMELLITATE (UNII: FY36J270ES)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    SORBITOL (UNII: 506T60A25R)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MANNITOL (UNII: 3OWL53L36A)  
    SUCROSE (UNII: C151H8M554)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    CETYL ESTERS WAX (UNII: D072FFP9GU)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CHAMOMILE (UNII: FGL3685T2X)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-644-01120 g in 1 BOTTLE; Type 0: Not a Combination Product02/02/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D02/02/2017
    Labeler - Wal-Mart Stores Inc (051957769)