SMART CARE HAND SANITIZER 33 OZ- ethyl alcohol gel

Smart Care Hand Sanitizer 33 oz by

Drug Labeling and Warnings

Smart Care Hand Sanitizer 33 oz by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lantern Science 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 this product.

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), Isopropyl Alcohol, 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

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 99.99% OF MOST COMMON GERMS

Aloe Vera & Vitamin E

FAST & EFFECTIVE

DESIGNED IN U.S.A.

MADE IN CHINA

WWW.SMARTCAREUS.COM

QUESTIONS OR COMMENTS?

1-877-274-8358 TOLL FREE IN USA.

1-909-434-0911 INTERNATIONAL

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY

ASHTEL STUDIOS INC. ONTARIO, CALIFORNIA 91761

Packaging

INGREDIENTS AND APPEARANCE

SMART CARE HAND SANITIZER 33 OZ 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-193
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: 54860-193-01	1000 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 - Shenzhen Lantern Science Co., ltd. (421222423)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Science Co., ltd.		421222423	manufacture(54860-193)