CLARIO FOAMING ALCOHOL INSTANT HAND SANITIZER- alcohol soap

Clario Foaming Alcohol Instant Hand Sanitizer by

Drug Labeling and Warnings

Clario Foaming Alcohol Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Betco Corporation, Ltd., Betco corporation, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Clario Foaming Alcohol Instant Hand Sanitizer

​Active Ingredient

Ethyl Alcohol 62%

Clario Foaming Alcohol Instant Hand Sanitizer

Uses

• Use hand sanitizer to reduce microorganisms on the skin.
• Use this product when soap and water are not available.

Clario Foaming Alcohol Instant Hand Sanitizer

Warnings

• For external use only.
• FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition.
• Children under the age of 6 should be supervised by an adult when using this product.
• Discontinue use is irritation or redness develops.
• KEEP OUT OF REACH OF CHILDREN.

Clario Foaming Alcohol Instant Hand Sanitizer

Directions

• ​Read the entire label before using this product.
• ​Dispense 0.8 mL of product onto dry hands. Rub hands together until hands are dry.
• Use as needed between hand washes to help reduce bacteria on the skin.

Clario Foaming Alcohol Instant Hand Sanitizer

Inactive Ingredients

​Water, Alkyl Phosphate Salts, PEG-10 Dimethicone, Propylene Glycol, Fragrance, D&C Green #5.

Clario Foaming Alcohol Instant Hand Sanitizer

Questions or Comments?Phone: (800) 777-9343

MDS information:​(800) 891-4965

Clario Foaming Alcohol Instant Hand Sanitizer

Purpose

Antiseptic

Clario Foaming Alcohol Instant Hand Sanitizer

KEEP OUT OF REACH OF CHILDREN

Clario Foaming Alcohol Instant Hand Sanitizer

Clario Foaming Alcohol Instant Hand Sanitizer

Alcohol Based Foaming Hand Sanitizer

Net Contents: 1000 mL

Item #77429-00

MSDS No. 774

2010 Beto Corporation

Toledo, Ohio 43607-0127 Made in U.S.A.

All Rights Reserved. www.betco.com

INGREDIENTS AND APPEARANCE

CLARIO FOAMING ALCOHOL INSTANT HAND SANITIZER 
alcohol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65601-774
Route of Administration	Topical

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIETHANOLAMINE (UNII: AZE05TDV2V)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65601-774-29	1000 mL in 1 BAG
2	NDC: 65601-774-53	50 mL in 1 BOTTLE, PUMP
3	NDC: 65601-774-57	550 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/12/2012

Labeler - Betco Corporation, Ltd. (005050158)

Registrant - Betco corporation, Ltd. (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd.		005050158	manufacture(65601-774)