Label: END-ZIT- sulfur lotion, augmented

  • NDC Code(s): 68605-2001-2, 68605-2002-2, 68605-2010-2
  • Packager: ABBE Laboratories, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 1, 2023

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  • 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   Acne Control Mask 68605-2010-2

  • ———PACKAGE LABEL.PRINCIPAL DISPLY 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
  • ———PACKAGE LABEL.PRINCIPAL DISPLY 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
  • ———PACKAGE LABEL.PRINCIPAL DISPLY 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 TypeHUMAN OTC DRUGItem Code (Source)NDC:68605-2001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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
    Colorbrown (Light/Medium) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68605-2001-214.78 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product04/20/2004
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug333D04/20/2004
    END-ZIT 
    sulfur lotion, augmented
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68605-2002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR.05 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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
    Colorbrown (Medium/Dark) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68605-2002-217.57 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product04/20/2004
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug333D04/20/2004
    END-ZIT 
    sulfur lotion, augmented
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68605-2010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR.05 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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
    Colorwhite (Mask) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68605-2010-270 g in 1 TUBE; Type 0: Not a Combination Product04/20/2004
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug333D04/20/200410/31/2023
    Labeler - ABBE Laboratories, Inc. (781745286)
    Establishment
    NameAddressID/FEIBusiness Operations
    ABBE Laboratories, Inc.781745286manufacture(68605-2001, 68605-2002, 68605-2010)
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