SMART CARE SUGAR COOKIE HAND SANITIZER- ethyl alcohol spray

Smart Care SUGAR COOKIE HAND SANITIZER by

Drug Labeling and Warnings

Smart Care SUGAR COOKIE 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
   Apply the spray to your hands and rub them together until dry. Recommended for repeated use.
Children under 6 years of age
   Supervision recommended 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, Blue 1, Denatonium Benzoate, Fragrance, Glycerin, PEG-40 Hydrogenated Castor Oil, Red 33, Tocopheryl Acetate, Water, Yellow 5

Questions or comments?

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

SCENTED & POCKET-FRIENDLY
KILLS UP TO 99% OF GERMS*

MADE IN CHINA

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

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

Smart Care® SMARTCAREUS.COM
COMMENTS? / QUESTIONS? / COMMENTAIRES?
1-909-434-0911 INTERNATIONAL

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

Packaging

INGREDIENTS AND APPEARANCE

SMART CARE SUGAR COOKIE HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-099
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)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
GLYCERIN (UNII: PDC6A3C0OX)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70108-099-01	1 in 1 POUCH	09/01/2024
1		40 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)	09/01/2024

Labeler - Ashtel Studios Inc. (148689180)