SMART CARE HOT WHEELS HAND SANITIZER- ethyl alcohol spray

Smart Care Hot Wheels HAND SANITIZER by

Drug Labeling and Warnings

Smart Care Hot Wheels HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Ashtel Studios, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

Decreases bacteria on skin

Warnings

For external use only

Flammability. Keep away from fire or flame.

Do not use
If you are allergic to any of the ingredients

When using this product Do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor If irritation or rash develops and continues for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 6 years and older
   Spray onto hands and rub together until dry. Recommended for repeat use.
Children under 6 years of age
   should be supervised when using this product.

Other Information

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Gel, Aminomethyl Propanol, Denatonium Benzoate, Fragrance, Glycerin, Tocopheryl Acetate, Water.

Questions or comments?

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

*Effective at killing 99.9% Escherichia coli, Staphylococcus aureus.

HOTWHEELS.COM
HOT WHEELSTM and associated trademarks and trade dress are owned by, and used under license from, Mattel. ©2024 Mattel.

DESIGNED IN U.S.A.
MANUFACTURED IN CHINA

Smart Care®
WWW.SMARTCAREUS.COM
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 HOT WHEELS HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-085
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70108-085-01	3 in 1 BOX	06/15/2024
1		28 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/15/2024

Labeler - Ashtel Studios, Inc. (148689180)