SMART CARE HAND SANITIZER 2 OZ- ethyl alcohol gel

Smart Care Hand Sanitizer 2 oz by

Drug Labeling and Warnings

Smart Care Hand Sanitizer 2 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 Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

To help reduce bacteria and germs on the skin.

WARNING

• Flammable. Keep away from fire or flame. For external use only
• Stop use and ask a doctor if irritation or redness develops and persists.

Keep out of reach of children

In case of accidental digestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

• Place enough product in palm to cover hands and rub hands together briskly until dry.
• Children under 6, use only under adult supervision.
• 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

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

QUESTIONS OR COMMENTS?

1-877-274-8358 Toll Free in USA. 1-909-434-0911 International

COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY ASHTEL STUDIOS INC. ONTARIO, CALIFORNIA 91761

Packaging

INGREDIENTS AND APPEARANCE

SMART CARE HAND SANITIZER 2 OZ 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-192
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 (UNII: H4N855PNZ1)
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: 54860-192-01	59 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(54860-192)