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Magic Marker (CoValence Inc.)

Available Formats

Dosage Form Package Information Links
GEL 1 TUBE in 1 CARTON (66915-436-01) > 36 g in 1 TUBE (66915-436-04) Label Information
GEL 7.5 g in 1 JAR (66915-436-03) Label Information
GEL 200000 g in 1 DRUM (66915-436-02) Label Information

Complete Magic Marker Information

  • DOSAGE & ADMINISTRATION

    Directions
    • Clean Skin thoroughly before applying this product.
    • Cover the entire affected area with a thin layer 1 to 3 times daily.
    • Because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 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.
    • Sensitivity Test for a New User; Apply product sparingly to one or two small affected areas during the first 2 days.  If no discomfort occurs, follow the directions stated elsewhere on this label.

  • ACTIVE INGREDIENT

    Active Ingredient:   Benzoyl Peroxide 5%


  • PURPOSE

    Uses

    • for the treatment of acne
    • helps clear up acne blemishes
    • helps prevent new acne blemishes from forming

  • WARNINGS

    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

    Do not use if you

    • have very sensitive skin.
    • are sensitive to benzoyl peroxide

  • WHEN USING

    When using this product

    • avoid unnecessary skin exposure and use a sunscreen
    • avoid contact with eyes, lips and mouth.  If eye contact accidentally occurs, rinse eyes throughly with water.
    • 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.


  • INACTIVE INGREDIENT

    Inactive Ingredients Aqua (Water), Glycerin, Allantoin, Aloe Barbadensis Leaf Juice Powder*, Acrylates/C13-30 Alkyl Acrylate Crosspolymer, Sorbitol, Sodium Hydroxide, Caprylyl Glycol, Phenoxethanol *Certified Organic


  • KEEP OUT OF REACH OF CHILDREN

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


  • INDICATIONS & USAGE

    Acne Treatment Step 2. Treat
    • Budhi Acne Treatment, 5% Benzoyl Peroxide, helps kill bacteria, dry up acne blemishes and prevent new ones from forming
    • Specifically formulated for teens
    • Penetrates pores to help fight the Propionibacterium acnes bacteria that can cause acne
    • Benzoyl peroxide is considered the most effective over-the-counter drug for the treatment of acne
    • Effictive for back acne or "Backne"
    • Certified organic aloe vera soothes and aids in healing irritated skin
    • Allantoin is an effective anti-irritant that promotes healthy cell renewal.
    • No parabens, sodium lauryl/lauthreth sulfates, phthalates, alcohol, witch hazel or dyes
    • No potentially irritating essential oils
    • Gluten free
    • Fragrance free

  • PRINCIPAL DISPLAY PANEL

    budhi Teencare acne treatment
    Outer Carton

  • INGREDIENTS AND APPEARANCE
    MAGIC MARKER 
    benzoyl peroxide gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66915-436
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Benzoyl Peroxide (UNII: W9WZN9A0GM) (Benzoyl Peroxide - UNII:W9WZN9A0GM) Benzoyl Peroxide 52.5 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Allantoin (UNII: 344S277G0Z)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Carbomer Copolymer TYPE A (UNII: 71DD5V995L)  
    Sorbitol (UNII: 506T60A25R)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Caprylyl Glycol (UNII: 00YIU5438U)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66915-436-01 1 in 1 CARTON
    1 NDC:66915-436-04 36 g in 1 TUBE
    2 NDC:66915-436-02 200000 g in 1 DRUM
    3 NDC:66915-436-03 7.5 g in 1 JAR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 08/09/2010
    Labeler - CoValence Inc. (070659375)
    Establishment
    Name Address ID/FEI Business Operations
    CoValence Inc. 070659375 manufacture