ANTIBACTERIAL SKIN CLEANSER 82- chloroxylenol soap

Antibacterial Skin Cleanser 82 by

Drug Labeling and Warnings

Antibacterial Skin Cleanser 82 by is a Otc medication manufactured, distributed, or labeled by Whisk Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Active Ingredient

Chloroxylenol 1% w/w

​Purpose

Health Care Personnel Hand Wash  

​Uses

• Hand wash to help reduce bacteria that cause disease
• Repeated usage suggested

Warnings

​For external use only.
Aovid contact with eyes and mouth.
If redness or irritation develops, discontinue use immediately. If condition persists more than 72 hours, consult a physician.

Keep out of reach of children.
Not for use on children under 6 months of age.

​Directions

• Wet hands and forearms.
• Apply 5 mL of product to hands.
• Scrub well for 30 seconds.
• Rinse and repeat.

​Inactive Ingredients

Water, Sodium C14-16 Olefin Sulfonate, Sodium Laureth Sulfate, Lauramide DEA, Isopropyl Alcohol, Polyquaternium-7, Fragrance, Styrene/Acrylates Copolymer, Tetrasodium EDTA, Citric Acid

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL SKIN CLEANSER 82 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65585-579
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
LAURIC DIETHANOLAMINE (UNII: O4GQ19886U)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Characteristics
Color	white (white, opaque liquid)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65585-579-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/20/2016

Labeler - Whisk Products, Inc. (834270639)

Establishment
Name	Address	ID/FEI	Business Operations
Whisk Products, Inc.		834270639	manufacture(65585-579)