XTRACARE FOAM ANTIBACTERIAL HAND WASH REFILL VANILLA PASSION FLOWER- benzalkonium chloride liquid 
China Ningbo Shangge Cosmetic Technology Corp

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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XtraCare Foam Antibacterial Hand Wash

Active Ingredient                                    Purpose

Benzalkonium Chloride 0.1% ............. Antibacterial

Uses

for hand washing to decrease bacteria on the skin

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

XtraCare® Foam Antibacterial HAnd Wash

Kills 99.9% of bacteria

Refill

Compare to Lysol foam antibacterial hand wash

vanilla passion flower

15 Fl Oz (444mL)

Warnings

For external use only

When using this product avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if irritation and redness develops.

Directions

Inactive Ingredients

water, glycerin, lauramine oxide, PEG-150 distearate, cetrimonium chloride, propylene glycol, fragrance, citric acid, tetrasodium EDTA, cocamide MEA, methylchloroisothiazolinone, methylisothiazolinone, D&C red no.33, FD&C blue no.1

Other Information

store at room temperature

Questions/Comments? 1-855-345-5575

*this product is not manufactured or distributed by Reckitt Benckiser LLC, the distributor of Lysol® foam antibacterial hand wash.

DISTRIBUTED BY: 

REJOICE INTERNATIONAL INC

NORTHVILLE, MI 48168, USA

MADE IN CHINA

label image

XTRACARE FOAM ANTIBACTERIAL HAND WASH  REFILL VANILLA PASSION FLOWER
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58503-045
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.5 g  in 444 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58503-045-01444 g in 1 BOTTLE; Type 0: Not a Combination Product01/24/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/24/2014
Labeler - China Ningbo Shangge Cosmetic Technology Corp (529287434)
Establishment
NameAddressID/FEIBusiness Operations
China Ningbo Shangge Cosmetic Technology Corp529287434manufacture(58503-045)

Revised: 9/2019
Document Id: 926fa735-4a45-981e-e053-2995a90a7da9
Set id: 9d83a452-f6ce-43ba-a744-844814c858d2
Version: 2
Effective Time: 20190913
 
China Ningbo Shangge Cosmetic Technology Corp