SMART CARE HAND SANITIZER 8 OZ- ethyl alcohol gel

Smart Care Hand Sanitizer 8 oz by

Drug Labeling and Warnings

Smart Care Hand Sanitizer 8 oz by is a Otc medication manufactured, distributed, or labeled by Yozzi Co.,ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Ethyl Alcohol 62%

Purposes

Antiseptic

Uses

For external use only: hands

Directions

Put a thumbnail size amount in your palm and rub your hands together briskly until dry. Children under 6 years of age should be supervised when using SMART CARE® HAND SANITIZER. Not recommended for infants.

Other Information

▪ Do not store above 100°F (38°C).
▪ May discolor some fabrics.
▪ Harmful to wood finishes and plastics.

Inactive Ingredients

Water (Aqua), Aloe Barbadensis Leaf Extract, Carbomer, Parfum, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine, FD&C Yellow No. 5(Tartrazine), FD&C Blue No. 1

Warnings:

For external use only: hands

Flammable. Keep away from fire or flame. 

When using this product

▪ Keep out of eyes.

▪ In case of contact with eyes, flush thoroughly with water.

▪ Avoid contact with broken skin.

▪ Do not inhale or ingest.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

SPL UNCLASSIFIED SECTION

KILLS UP TO 99.9% OF MOST COMMON GERMS

Aloe Vera & Vitamin E

FAST & EFFECTIVE

SMARTCAREUS.COM

QUESTIONS OR COMMENTS?

1-877-274-8358 TOLL FREE IN U.S.A.

1-909-434-0911 INTERNATIONAL

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY ASHTEL STUDIOS INC. ONTARIO, CALIFORNIA 91761

DESIGNED IN U.S.A. MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

SMART CARE HAND SANITIZER 8 OZ 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72285-002
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
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: 72285-002-01	236.6 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/06/2020

Labeler - Yozzi Co.,ltd (560426393)

Establishment
Name	Address	ID/FEI	Business Operations
Yozzi Co.,ltd		560426393	manufacture(72285-002)