SMART CARE HAND SANITIZER SWEET CITRUS- ethyl alcohol spray

Smart Care HAND SANITIZER SWEET CITRUS by

Drug Labeling and Warnings

Smart Care HAND SANITIZER SWEET CITRUS 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

Flammable, 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 them together until dry. Recommended for repeated use.

Children under 6 years of age
  Should be supervised when using this product.

Other information

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

Inactive ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Gel, Aminomethyl Propanol, Denatonium Benzoate, Fragrance, Glycerin, PEG-40 Hydrogenated Castor Oil, Red 4, Tocopheryl Acetate, Water, Yellow 5

Questions or comments?

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

*Effective at killing 99.9% of Escherichia coli, Staphylococcus aureus under laboratory settings

Smart Care® SMARTCAREUS.COM
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 SWEET CITRUS 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-144
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)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
.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: 70108-144-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/15/2025

Labeler - Ashtel Studios, Inc. (148689180)