END-ZIT- sulfur lotion, augmented

END-ZIT by

Drug Labeling and Warnings

END-ZIT by is a Otc medication manufactured, distributed, or labeled by ABBE Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

———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)

———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)

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; Type 0: Not a Combination Product	04/20/2004

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; Type 0: Not a Combination Product	04/20/2004

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: 68605-2010
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 (Mask)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68605-2010-2	70 g in 1 TUBE; Type 0: Not a Combination Product	04/20/2004

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(68605-2001, 68605-2002, 68605-2010)