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END-ZIT (ABBE Laboratories, Inc.)

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LOTION, AUGMENTED 14.78 mL in 1 BOTTLE, GLASS (68605-2001-2) Label Information

Complete END-ZIT Information

  • INDICATIONS & USAGE

    Intended for use on blemishes only. This advanced formulation is designed to dry and aid in elimination of pimples. It is make-up quality for excellent coverage of the blemish. It is unbelievably effective, clinically tested, dermatologist approved and recommended.


  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Shake bottle well before each use. Apply directly to blemish only, using applicator. Wait a few moments until slightly dry. Pat with fingertip or clean cotton swab to blend color to skin. Make-up may be applied if desired. Should remain on skin all day. Re-apply at night to clean skin to remain on skin overnight.


  • DO NOT USE

    NOTE: PERSONS WITH KNOWN SENSITIVITY TO SULFUR SHOULD AVOID USE OF THIS PRODUCT.
    KEEP FROM EYES.


  • ACTIVE INGREDIENT

    DRUG  FACTS
    ACTIVE INGREDIENT ............  SULFUR 5%


  • PURPOSE

    PURPOSE    .............    ACNE TREATMENT


  • WARNINGS

    WARNINGS:
    For external use only.
    Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
    Do not get into eyes. If excessive skin irritation deve lops or increases, discontinue use and consult a doctor.


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.


  • INACTIVE INGREDIENT

    OTHER INGREDIENTS: Isopropyl Alcohol, Water, Zinc Oxide, Propylene Glycol, Camphor, Talc, Sodium Laureth Sulfate, Titanium Dioxide, Diazolidinyl Urea, Methylparaben, Propylparaben. May contain Iron Oxides.

    NDC #'s
    Light/Medium 68605-2001-2       Medium/Dark 68605-2002-2
    Sun Bronze 68605-2003-2                  Untinted 68605-2006-2


  • PRINCIPAL DISPLAY PANEL

    DIRECTIONS: SHAKE BOTTLE WELL.
    APPLY TWICE DAILY DIRECTLY TO
    ACNE BREAKOUT. ALLOW TO DRY
    FOR 10 SECONDS. PAT TO BLEND.
    APPLY MAKE-UP IF DESIRED.

    ACTIVE INGREDIENT: SULFUR 5%.

    WARNINGS:
    AVOID IF ALLERGIC TO SULFUR
    AVOID CONTACT WITH EYES
    FOR EXTERNAL USE ONLY
    KEEP FROM CHILDREN

    Manufactured by ABBE Laboratories, Inc.
    Farmingdale, NY 11735
    Made in the U.S.A.

    END-ZIT®

    ACNE CONTROL
    DRYING LOTION

    ABBE

    0.62 OZ. (17.57 g)

    Product Label


  • INGREDIENTS AND APPEARANCE
    END-ZIT 
    sulfur lotion, augmented
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68605-2001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR .05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    TALC (UNII: 7SEV7J4R1U)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Product Characteristics
    Color brown (Light/Medium) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68605-2001-2 14.78 mL in 1 BOTTLE, GLASS
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 04/20/2004
    END-ZIT 
    sulfur lotion, augmented
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68605-2002
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR .05 g  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    TALC (UNII: 7SEV7J4R1U)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Product Characteristics
    Color brown (Medium/Dark) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68605-2002-2 17.57 g in 1 BOTTLE, GLASS
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 04/20/2004
    END-ZIT 
    sulfur lotion, augmented
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68605-2003
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR .05 g  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    TALC (UNII: 7SEV7J4R1U)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Product Characteristics
    Color brown (Sun Bronze) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68605-2003-2 17.57 g in 1 BOTTLE, GLASS
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 04/20/2004
    END-ZIT 
    sulfur lotion, augmented
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68605-2006
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR .05 g  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    TALC (UNII: 7SEV7J4R1U)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Product Characteristics
    Color white (Untinted) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68605-2006-2 17.57 g in 1 BOTTLE, GLASS
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 04/20/2004
    Labeler - ABBE Laboratories, Inc. (781745286)
    Establishment
    Name Address ID/FEI Business Operations
    ABBE Laboratories, Inc. 781745286 manufacture