JOJO SIWA HAND SANITIZER 0.84 OZ- ethyl alcohol gel

Jojo Siwa Hand Sanitizer 0.84 oz by

Drug Labeling and Warnings

Jojo Siwa Hand Sanitizer 0.84 oz 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 Ingredients

Ethyl Alcohol 62%

Purposes

Antimicrobial

Uses

To help reduce bacteria and germs on the skin.

Warnings

Flammable. Keep away from fire or flame.

For external use only: hands

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Put a thumbnail size amount in your palm and rub your hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product.

Other Information

▪ Store below 110°F (43°C).

▪ May discolor certain fabrics or surfaces.

▪ Harmful to wood finishes and plastics.

Inactive Ingredients

Water, Glycerin, Carbomer, Green-Tea extract, Mugwort extract, Sponge Cucumber Gourd extract, L-menthol, Triethanolamine

SPL UNCLASSIFIED SECTION

Do Not Eat

Clean Hands

DREAMER

KILLS 99% OF GERMS

Moisturizing Effect

Our Hygienic Hand Sanitizer has a moisturizing effect with Sponge Cucumber Gourd extract and protects dry skin with green-tea extract.

© 2020 Viacom International Inc. All Rights Reserved.

Nickelodeon and all related titles and logos are trademarks of Viacom International Inc. JoJo Siwa is a trademark of JoJo Siwa Entertainment, LLC.

DESIGNED IN U.S.A. MADE IN KOREA

WWW.SMARTCAREUS.COM

QUESTIONS OR COMMENTS?

1-877-274-8358 TOLL FREE IN U.S.A.

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

JOJO SIWA HAND SANITIZER 0.84 OZ 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-044
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
LUFFA AEGYPTIACA FRUIT (UNII: QKL9NEO1F9)
LEVOMENTHOL (UNII: BZ1R15MTK7)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70108-044-01	25 mL in 1 POUCH; Type 0: Not a Combination Product	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/06/2020

Labeler - Ashtel Studios, Inc (148689180)