ALCOHOL FOAMING HAND SANITIZER- alcohol soap

Alcohol Foaming Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Uses

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

Warnings

• For external use only. Do not ingest.
• FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition.
• Avoid contact with eyes. In case of eye contact, flush with large quantities of water, seek medical attention if irritation persists.
• If skin irritation develops, discontinue use. If irritation persists for more than 72 hours, seek medical attention.
• Keep out of reach of children.
• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• ​Read the entire label before using this product.
• ​Dispense 2 pumps of product onto palm of hand and rub thoroughly over all surfaces of both hands until dry.

Inactive Ingredients

Water, Propylene Glycol, Acrylic Polymer, Alkyl Phosphate Salts, Fragrance, DC Green #5.

Purpose

Antiseptic

Alcohol Foaming Hand Sanitizer

KEEP OUT OF REACH OF CHILDREN

Alcohol Foaming Hand Sanitizer

755_AlcoholFoamingHandSanitizer_

INGREDIENTS AND APPEARANCE

ALCOHOL FOAMING HAND SANITIZER 
alcohol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65601-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65601-701-04	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2016
2	NDC: 65601-701-05	1200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/15/2016
3	NDC: 65601-701-53	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2016
4	NDC: 65601-701-57	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2016
5	NDC: 65601-701-29	1000 mL in 1 BAG; Type 0: Not a Combination Product	06/01/2016
6	NDC: 65601-701-03	750 mL in 1 BAG; Type 0: Not a Combination Product	09/15/2016
7	NDC: 65601-701-55	208198 mL in 1 DRUM; Type 0: Not a Combination Product	06/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/01/2016

Labeler - Betco Corporation, Ltd. (024492831)

Registrant - Betco Corporation, Ltd. (024492831)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd.		024492831	manufacture(65601-701) , label(65601-701)