SMART CARE SPIDER-MAN HAND SANITIZER- ethyl alcohol spray

Smart Care SPIDER-MAN HAND SANITIZER by

Drug Labeling and Warnings

Smart Care SPIDER-MAN 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

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, call Poison Help at 1-800-222-1222 or go to PoisonHelp.org.

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, Blue 1, Denatonium Benzoate, Fragrance, Glycerin, PEG-40 Hydrogenated Castor Oil, Tocopheryl Acetate, Water, Yellow 5

Questions or comments?

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

MARVEL

THE AMAZING SPIDER-MAN

KILLS UP TO 99.9% OF MOST COMMON GERMS*

GHOST SHOOTER SCENT

MADE IN CHINA

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

© MARVEL

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 SPIDER-MAN HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-264
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)
.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: 70108-264-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/07/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/07/2025

Labeler - Ashtel Studios, Inc. (148689180)