HAND SANITIZER-SPRAY- alcohol spray

Hand sanitizer-spray by

Drug Labeling and Warnings

Hand sanitizer-spray by is a Otc medication manufactured, distributed, or labeled by Landy International, Snoozy Freshners, LLC, DM imports, Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

PEG-40 hydrogenated castor oil, Fragrance (Parfum), Tocopheryl acetate, Aloe barbadensis leaf extract, Phenoxyethanol, Ethylhexylglycerin, purified water USP

Package Label - Principal Display Panel

60 mL NDC: 51706-814-01

60 mL NDC: 51706-814-02

60 mL NDC: 51706-814-03

60 mL NDC: 51706-814-04

PRINCIPAL DISPLAY PANEL

60 mL NDC: 51706-815-01

60 mL NDC: 51706-815-02 60 mL NDC: 51706-815-03

60 mL NDC: 51706-815-04

PRINCIPAL DISPLAY PANEL

60ml NDC: 51706-816

INGREDIENTS AND APPEARANCE

HAND SANITIZER-SPRAY 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51706-814
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
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.0003 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51706-814-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 51706-814-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 51706-814-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 51706-814-04	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/30/2020

HAND SANITIZER-SPRAY 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51706-816
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
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.0003 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51706-816-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 51706-816-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 51706-816-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 51706-816-04	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/30/2020

HAND SANITIZER-SPRAY 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51706-815
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
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.0003 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51706-815-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 51706-815-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 51706-815-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 51706-815-04	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/30/2020

Labeler - Landy International (545291775)

Establishment
Name	Address	ID/FEI	Business Operations
Snoozy Freshners, LLC		075299630	label(51706-814)

Establishment
Name	Address	ID/FEI	Business Operations
Landy International		545291775	manufacture(51706-814, 51706-815, 51706-816)

Establishment
Name	Address	ID/FEI	Business Operations
DM imports, Ltd		799543041	label(51706-815)