HELLO KITTY BY SANRIO HAND SANITIZER- ethyl alcohol solution

Hello Kitty by Sanrio Hand Sanitizer by

Drug Labeling and Warnings

Hello Kitty by Sanrio Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by 4e Brands Northamerica LLC, 4E Global, S.A.P.I. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

ACTIVE INGREDIENT

Ethyl alcohol

PURPOSE

Antimicrobial

USES

For hand washing to decrease bacteria on the skin. Recommended for repeated use.

WARNINGS

For external use only. Flammable. Keep away from heat and flame.

When using this product

avoid contact with eyes. If contact occurs, flush eyes with water. Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

Keep out of the reach of children

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

Directions

Wet hands thoroughly with product and allow to dry without wiping.

For children under 6, use only under adult supervision.

Not recommended for infants.

Repeat as necessary.

Other information

Do ot store above 105F

May discolor some fabrics. Harmful to wood finishes and plastics.

Inactive Ingredients

Water, Carbomer, Glycerin, Fragrance, Castor Oil, Triethanolamine, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis Leaf  Extract (Aloe Vera)

SPL UNCLASSIFIED SECTION

Distributed by 4e Brands North America, LLC 17806

1H 10W Suite 300, San Antonio, TX 78257

4ebrands.com

made in Mexico

Package labeling

INGREDIENTS AND APPEARANCE

HELLO KITTY BY SANRIO HAND SANITIZER 
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70074-802
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CASTOR OIL (UNII: D5340Y2I9G)
TROLAMINE (UNII: 9O3K93S3TK)
TOCOPHEROL (UNII: R0ZB2556P8)
ALOE (UNII: V5VD430YW9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70074-802-00	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/21/2015

Labeler - 4e Brands Northamerica LLC (076595687)

Registrant - 4E Global, S.A.P.I. de C.V. (812821307)

Establishment
Name	Address	ID/FEI	Business Operations
4E Global, S.A.P.I. de C.V.		812821307	manufacture(70074-802)