END-ZIT  - sulfur lotion, augmented 
ABBE Laboratories, Inc.

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END-ZIT® ACNE CONTROL DRYING LOTION

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.

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.

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

DRUG  FACTS
ACTIVE INGREDENT ............  SULFUR 5%

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

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.

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
Brown 68605-2004-2
Medium/Dark 68605-2005-2

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)

END-ZIT  sulfur   lotion, augmented

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 68605-2004 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (SULFUR) SULFUR .05 g  in 1 g

Inactive Ingredients Ingredient Name Strength ISOPROPYL ALCOHOL   WATER   ZINC OXIDE   PROPYLENE GLYCOL   CAMPHOR (SYNTHETIC)   TALC   SODIUM LAURETH SULFATE   TITANIUM DIOXIDE   DIAZOLIDINYL UREA   METHYLPARABEN   PROPYLPARABEN

Product Characteristics Color brown Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 68605-2004-2 17.57 g In 1 BOTTLE, GLASS None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	04/20/2004	02/28/2008

END-ZIT  sulfur   lotion, augmented

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 68605-2005 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (SULFUR) SULFUR .05 g  in 1 g

Inactive Ingredients Ingredient Name Strength ISOPROPYL ALCOHOL   WATER   ZINC OXIDE   PROPYLENE GLYCOL   CAMPHOR (SYNTHETIC)   TALC   SODIUM LAURETH SULFATE   TITANIUM DIOXIDE   DIAZOLIDINYL UREA   METHYLPARABEN   PROPYLPARABEN

Product Characteristics Color brown (Medium/Dark) Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 68605-2005-2 17.57 g In 1 BOTTLE, GLASS None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	04/20/2004	02/28/2008

Labeler - ABBE Laboratories, Inc. (781745286)

Establishment
Name	Address	ID/FEI	Operations
ABBE Laboratories, Inc.		781745286	manufacture

Revised: 03/2011ABBE Laboratories, Inc.