SANIWASH ANTIMICROBIAL FOAMING HAND- chloroxylenol liquid 
Safetec of America, Inc.

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61010-8600-1, SaniwashAntimicrobial Foming Hand

Active Ingredient

Chloroxylenol (PCMX)

Purpose

Antiseptic

Uses

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 ifirritation 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

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

18.6 fl. Oz (550 ml)

PRINCIPAL DISPLAY PANEL -18.6 fl. oz
SANIWASH ANTIMICROBIAL FOAMING HAND 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61010-8600
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.006 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61010-8600-1550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/13/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)03/13/2014
Labeler - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIBusiness Operations
Safetec of America, Inc874965262manufacture(61010-8600)

Revised: 2/2024
Document Id: 1095825e-527e-d9f5-e063-6394a90af140
Set id: bab4ca5f-01c6-4146-b18f-c22cbe0fe13b
Version: 4
Effective Time: 20240204
 
Safetec of America, Inc.