Label: UNBLEMISH DUAL INTENSIVE ACNE TREATMENT- benzoyl peroxide lotion

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

Drug Label Information

Updated December 9, 2024

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

  • Active Ingredients

    Benzoyl Peroxide 2.5%

  • Purpose

    Acne treatment

  • Uses

    • For the treatment of acne.
    • Helps keep skin clear of new acne blemishes, acne pimples, blackheads, and whiteheads.
  • 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 occurs, only use one topical acne medication at a time.

    Do not use if you

    • Have very sensitive skin.
    • Are sensitive to benzoyl peroxide.

    When using this product

    • Avoid unnecessary sun exposure and use a sunscreen
    • Avoid contact with the eyes, lips, and mouth
    • Avoid contact with hair and dyed fabrics, which may be bleached by this product
    • Skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

    Stop use and ask a doctor if

    • Irritation becomes severe

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

  • Directions

    • Clean the skin thoroughly before applying this product. Dispense 1-2 pumps from each side. Blend product evenly. Cover the entire affected area with a thin even layer one to three times daily. Do not rinse product off face.
    • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
    • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
    • If going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
    • Wash hands after application to help avoid staining fabrics.
  • Other Information

    Store between 15-30°C (59-86°F).

  • Inactive Ingredients

    Water, Ethoxydiglycol, Glycerin, Polyacrylamide, Chamomilla Recutita (Matricaria) Flower Extract, Aloe Barbadensis Leaf Juice, Allantoin, Niacinamide, Panthenol, Punica Granatum Fruit Extract, Yucca Glauca Root Extract, Ceramide AP, Ceramide EOP, Ceramide NP, Fragrance (Parfum), Biosaccharide Gum-1, Disodium Cocamido MIPA-Sulfosuccinate, Carbomer, Cholesterol, Leuconostoc/Radish Root Ferment Filtrate, Corn Starch Modified, Phytosphingosine, Sodium Lauroyl Lactylate, Xanthan Gum, Laureth-7, Aminomethyl Propanol, Disodium Oleamido MEA-Sulfosuccinate, Cl3-14 lsoparaffin, PEG-7 Glyceryl Cocoate, BHT, Disodium EDTA, Ethylhexylglycerin, Benzyl Alcohol, Phenoxyethanol, Citronellol, Geraniol, Limonene, Linalool

  • Questions

    1-888-995-5656

  • Principal Display Panel - 45mL / 1.5 Fl. Oz. Carton Label

    RODAN+FIELDS

    UMBLEMISH

    3 Dual Intensive
    Acne Treatment

    RODAN+FIELDS

    2 x 22.5 mL/0.76 Fl. Oz. U.S.

    Principal Display Panel - 45mL / 1.5 Fl. Oz. Carton Label
  • Principal Display Panel - 45mL / 1.5 Fl. Oz. Tube Label

    RODAN+FIELDS

    UMBLEMISH

    3 Dual Intensive
    Acne Treatment

    Principal Display Panel - 45mL / 1.5 Fl. Oz. Tube Label
  • INGREDIENTS AND APPEARANCE
    UNBLEMISH DUAL INTENSIVE ACNE TREATMENT 
    benzoyl peroxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:14222-2120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    CERAMIDE 1 (UNII: 5THT33P7X7)  
    CERAMIDE AP (UNII: F1X8L2B00J)  
    CERAMIDE NP (UNII: 4370DF050B)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    DISODIUM OLEAMIDO MONOETHANOLAMINE SULFOSUCCINATE (UNII: 5M1101WGSY)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GERANIOL (UNII: L837108USY)  
    LAURETH-7 (UNII: Z95S6G8201)  
    LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
    POMEGRANATE (UNII: 56687D1Z4D)  
    SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    YUCCA GLAUCA ROOT (UNII: 1A15YBH7N1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:14222-2120-11 in 1 CARTON02/13/2019
    145 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00602/13/2019
    Labeler - Rodan & Fields (051659584)