BENZALKONIUM CHLORIDE- benzalkonium chloride liquid 
SANI PRODUCTS INC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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SANI SLIME ALCOHOL-FREE HAND SANITIZER WATERMELON

ACTIVE INGREDIENTS

BENZALKONIUM CHLORIDE 0.13%

PURPOSE

ANTIBACTERIAL

USES

PROVIDE HAND SANITIZING WHEN SOAP AND WATER NOT AVAILABLE

KILLS OR REDUCES 99.9% OF HARMFUL BACTERIA/GERMS

RECOMMENDED FOR REPEATED USE

WARNINGS

FOR EXTERNAL USE ONLY

AVOID CONTACT WIYH EYES

IF INGESTED, CONSULT WITH A PHYSICIAN

WARNINGS

KEEP OUT OF REACH OF CHILDREN 2 YRS OF AGE OR YOUNGER

DIRECTIONS

RUB PRODUCT ONTO HANDS AND ALLOW TO DRY

USE AS PART OF YOUR DAILY CLEANSING ROUTINE

NO RINSING REQUIRED

QUESTIONS

WWW.SANISLIME.COM

OTHER INFORMATION

DO NOT FREEZE

INACTIVE INGREDIENT

WATER, GLYCERIN, CARBOMER, POLYSORBATE 20, DIMETHICONE, PHENOXYETHANOL, CAPRYLYL GLYCOL, SORBIC ACID, TRIETHANOLAMINE

SANISLIME ALCOHOL FREE HAND SANITIZER WATERMELON

ALCOHOL FREE

BENZALKONIUM CHLORIDE LIQUID

WATERMELON

SANISLIME

ALCOHOL-FREE HAND SANITIZER

KILLS HARMFUL BACTERIA

8 OZ (250 ML)

SANI SLIME WATERMELON

BENZALKONIUM CHLORIDE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69402-012
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.13 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
TROLAMINE (UNII: 9O3K93S3TK)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
SORBIC ACID (UNII: X045WJ989B)  
WATER (UNII: 059QF0KO0R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
Product Characteristics
Color    Score    
ShapeSize
FlavorWATERMELONImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69402-012-01250 mL in 1 BOTTLE; Type 0: Not a Combination Product12/13/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/13/2014
Labeler - SANI PRODUCTS INC. (202754156)

Revised: 12/2014
Document Id: 0a1a4ca8-e3fa-161c-e054-00144ff8d46c
Set id: 0a1a4ca8-e3f9-161c-e054-00144ff8d46c
Version: 1
Effective Time: 20141213
 
SANI PRODUCTS INC.