BLIPPI HAND SANITIZER- ethyl alcohol gel

Blippi HAND SANITIZER by

Drug Labeling and Warnings

Blippi HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Yozzi Co.,ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Use:

To help reduce bacteria and germs on the skin.

WARNINGS:

For external use only: hands.

Flammable. Keep away from fire or flame.

When using this product:

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.  Do not inhale or ingest.

 Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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. Not recommended for infants.

Other Information:

Do not store above 100° F (38°C)

May discolor some fabrics.

Harmful to wood finishes & plastics.

Inactive Ingredients:

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Extract, Fragrance, Tocopheryl Acetate (Vitamin E), FD&C Blue No. 1

QUESTIONS OR COMMENTS?

1-877-274-8358 Toll Free in USA

1-909-434-0911 International

SPL UNCLASSIFIED SECTION

KILLS 99% OF MOST COMMON GERMS

Blippi® and ©2020
Kideo, Inc
All Rights Reserved

DESIGNED IN U.S.A.

MADE IN CHINA

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY
ASHTEL STUDIOS INC.
ONTARIO, CA 91761

SMARTCAREUS.COM

Packaging

INGREDIENTS AND APPEARANCE

BLIPPI HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72285-007
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)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72285-007-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/17/2020

Labeler - Yozzi Co.,ltd (560426393)

Establishment
Name	Address	ID/FEI	Business Operations
Yozzi Co.,ltd		560426393	manufacture(72285-007)