SANIWASH ANTIMICROBIAL FOAMING HAND- chloroxylenol liquid

Saniwash Antimicrobial Foaming Hand by

Drug Labeling and Warnings

Saniwash Antimicrobial Foaming Hand by is a Otc medication manufactured, distributed, or labeled by Safetec of America, Inc. , Safetec of America, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Chloroxylenol (PCMX)

Purpose

Antiseptic

Uses

• For hand washing to decrease bacteria on the skin.
• Recommended for repeated use

Warnings

For external use only.

When using this product

• supervise children under 6
• do not use in eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask doctor if irritation or redness develop and persists for more than 72 hours.

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away

Directions

Wet hands and forearms. Apply 5 millimeters (teaspoonful) or palmful to hand and forearm. Scrub thoroughly for 30 seconds. Rince and repeat.

Inactive ingredients

aloe vera, calblend clear surfactant blend, DMDM hydantoin, fragrance, propylene glycol, purified/deionized water, tetrasodium EDTA, vitamin E acetate

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL -18.6 fl. oz

NDC: 61010-8600-1

Safetec

Saniwash

Antimicrobial Foaming Hand Soap

Effective against germs

Cleans dirty hands yet gentle on skin

Mild pleasant fragrance with Aloe

Manufactured by

Safetec

Safetec of America, Inc

Buffalo, NY 14215

1-800-456-7077 www.safetec.com Reorder No. 34456 Net Contents

18.6 fl. Oz (550 ml)

INGREDIENTS AND APPEARANCE

SANIWASH ANTIMICROBIAL FOAMING HAND 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61010-8600
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q)	Chloroxylenol	0.0060 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Aloe Vera Leaf (UNII: ZY81Z83H0X)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
DMDM HYDANTOIN (UNII: BYR0546TOW)
Propylene Glycol (UNII: 6DC9Q167V3)
Water (UNII: 059QF0KO0R)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61010-8600-1	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/13/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/13/2014

Labeler - Safetec of America, Inc. (874965262)

Establishment
Name	Address	ID/FEI	Business Operations
Safetec of America, Inc		874965262	MANUFACTURE(61010-8600)