CARE TOUCH INSTANT HAND SANITIZER- ethyl alcohol gel

Care Touch INSTANT HAND SANITIZER by

Drug Labeling and Warnings

Care Touch INSTANT 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

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

• To decrease bacteria on the skin that could cause disease.
• Recommended for repeated use.
• Use anywhere without water.

Warnings

• For external use only-hands.
• Flammable. Keep away from heat and flame.
• Discontinue if skin becomes irritated and ask a doctor.

When using this product.

• Keep out of eyes, in case of contact with eyes, flush thoroughly with water.
• Do not inhale or ingest.
• Avoid contact with broken skin.

Keep out of reach of children.

Keep out of reach of children. In case of accidental ingestion. seek professional assisstance or control a Poison Control Centre immediately.

Directions

• Wet hands thoroughly h product and rub until dry without wiping
• For children 6, use only under adult supervision.
• Not recommended for infants.

Other Information

• Do not store above 105°F.
• May discolor some fabrics.
• Harmful to wood finishes and plastics.

Inactive Ingredients

Water, Isopropyl Aclohol, Glycerin, Carbomer, Aminomethyl Propanol, Parfum, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, FD&C Yellow No.5(Tartrazine), FD&C Blue No.1.

SPL UNCLASSIFIED SECTION

Care Touch®

INSTANT HAND SANITIZER SOOTHING GEL

KILLS 99.99% OF GERMS*

With Aloe And Vitamin E

This product as not tested on animals.

*kills 99.99% of most germs

Made in China for Future Diagnostics LLC

Brooklyn , NY 1120 1800.758.3830

caretouchusa.com

Packaging

INGREDIENTS AND APPEARANCE

CARE TOUCH INSTANT HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70393-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70393-004-67	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/22/2020
2	NDC: 70393-004-68	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/22/2020

Labeler - Future Diagnostics Llc (080113296)