SMART CARE HAND SANITIZER - CUCUMBER MELON FLAVOR- ethyl alcohol spray

Smart Care HAND SANITIZER - CUCUMBER MELON FLAVOR by

Drug Labeling and Warnings

Smart Care HAND SANITIZER - CUCUMBER MELON FLAVOR 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

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. 

Inactive ingredients

Water, Glycerin, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Tocopheryl Acetate, Aloe Barbadensis Gel, Denatonium Benzoate, Yellow 5, Blue 1

Questions or comments?

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

SCENTED & POCKET-FRIENDLY

KILLS UP TO 99% OF GERMS

A harmonious fusion of fresh cucumber and luscious melon. Indulge your senses and whisk away stress with each delicate spritz of our invigorating hand sanitizer.

Every airy mist ensures clean and nourished skin, providing a refreshing experience with each use.

Smart Care®    SMARTCAREUS.COM

1-909-434-0911 INTERNATIONAL

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY:
ASHTEL STUDIOS, INC.
ONTARIO, CALIFORNIA 91761

MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

SMART CARE HAND SANITIZER - CUCUMBER MELON FLAVOR 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-101
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
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: 70108-101-01	1 in 1 CARTON	07/29/2024
1		30 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)	07/29/2024

Labeler - Ashtel Studios Inc. (148689180)