CARETOUCH ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride liquid 
Future Diagnostics Llc

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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CareTouch® Alcohol-Free Foaming Hand Sanitizer

Drug Facts

Active ingredient

Benzalkonium chloride 0.1%

Purpose

Antibacterial

Uses

• For hand washing to decrease bacteria on the skin.

Warnings

For external use only.

When using this product if eye contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develops and persist 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

• Apply small amount of foam to hands as desired, allow drying without wiping.

Storage

• Store at room temperature

• Avoid direct sunlight.

Inactive ingredient

Water, Betaine Anhydrous, Diazolidinyl urea, Phenoxyethanol, Palmitamidopropyltrimonium Chloride, Propylene Glycol, Sodium Citrate

Alcohol-Free Moisturizing Formula

Kills 99.99% of Germs*

Fragrance-Free & Hypoallergenic

Free of Triclosan, Parabens, Sulfates, Phthalates

*Kills 99.99% of common, harmful germs in just 15 seconds.

NDC 70393-456-25

ITEM# CTAFF10

NDC 70393-456-04

ITEM# CTAFF10-4

NDC 70393-456-01

ITEM# CTAFFS-T1

ITEM# FHS48

NDC# 70393-456-80

1800.758.3830

caretouchusa.com

Manufactured in China for Future Brands Brooklyn, NY 11220

Packaging

sanitize1

image description

CARETOUCH ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70393-456
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BETAINE (UNII: 3SCV180C9W)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PALMITAMIDOPROPYLTRIMONIUM CHLORIDE (UNII: N2U96D202F)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70393-456-25300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2019
2NDC:70393-456-044 in 1 BAG03/01/2019
2NDC:70393-456-25300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:70393-456-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2020
4NDC:70393-456-088 in 1 PACKAGE03/15/2020
4NDC:70393-456-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:70393-456-8048 mL in 1 BOTTLE; Type 0: Not a Combination Product08/27/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/01/2019
Labeler - Future Diagnostics Llc (080113296)

Revised: 8/2020
Document Id: 6c264c06-50ac-4197-9a34-2ce25f75e890
Set id: c6989f81-889f-4451-ab44-9e6b6081898d
Version: 5
Effective Time: 20200827
 
Future Diagnostics Llc