CARETOUCH ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride liquid

CareTouch Alcohol-Free Foaming Hand Sanitizer by

Drug Labeling and Warnings

CareTouch Alcohol-Free Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Future Diagnostics Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

SPL UNCLASSIFIED SECTION

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

1800.758.3830

caretouchusa.com

Manufactured in China for Future Brands Brooklyn, NY 11220

Packaging

INGREDIENTS AND APPEARANCE

CARETOUCH ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70393-456
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70393-456-25	300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2019
2	NDC: 70393-456-04	4 in 1 BAG	03/01/2019
2	NDC: 70393-456-25	300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 70393-456-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2020
4	NDC: 70393-456-08	8 in 1 PACKAGE	03/15/2020
4	NDC: 70393-456-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/01/2019

Labeler - Future Diagnostics Llc (080113296)