HELLO KITTY BY SANRIO HAND SANITIZER- ethyl alcohol solution
4e Brands Northamerica LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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HELLO KITTY BY SANRIO HAND SANITIZER

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)

Distributed by 4e Brands North America, LLC 17806

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

4ebrands.com

made in Mexico

Package labeling

label

label 1

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

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:70074-802-00	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2015	07/07/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	08/21/2015	07/07/2020

Labeler - 4e Brands Northamerica LLC (076595687)

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

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

Revised: 12/2021

Document Id: d2ccbf36-199a-35d4-e053-2995a90ae22f

Set id: 276c987e-e714-4443-a137-e114e906ac41

Version: 5

Effective Time: 20211210

4e Brands Northamerica LLC