HAND SANITIZER 100 SINGLE USE VIALS X 1ML EA- belzalkonium chloride solution HAND SANITIZER 50 SINGLE USE VIALS X 1ML EA- benzalkonium chloride solution

Hand Sanitizer 50 Single Use Vials x 1mL ea by

Drug Labeling and Warnings

Hand Sanitizer 50 Single Use Vials x 1mL ea by is a Otc medication manufactured, distributed, or labeled by New Vision Pharmaceuticals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (s)

Belzalkonium Chloride 0.13%. Purpose: Antimicrobial

Purpose

Antimicrobial, Hand Sanitizer

Use

• Provide Hand sanitizing when soap and water are not available.
• Helps to kill or reduce harmful bacteria and germs.
• Recommended for repeated use.

Warnings

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes throughly with water

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children 2 years of age or younger.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

WHEN USING

When using this product do not use in or near the eyes. In case of contact, rinse eyes throughly with water

STOP USE

Stop use and ask a doctor if irritation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children 2 years of age or younger.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• Rub product into hands and allow to dry
• Use as part of your daily cleansing routine
• No rinsing required

Other information

• Do not freeze
• Store at a room temperature

Inactive Ingredients

aloe vera leaf extract, glucomannan 90% (Konjac), propylene glycol, purified water.

Package - Principal Display Panel

Hand Sanitizer

Single Use vials

100 Single Use vials x 1mL ea

Hand Sanitizer

Single Use vials

50 Single Use vials x 1mL ea

INGREDIENTS AND APPEARANCE

HAND SANITIZER 100 SINGLE USE VIALS X 1ML EA 
belzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70302-063
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
KONJAC MANNAN (UNII: 36W3E5TAMG)	0.002 g  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.1 g  in 1 mL
WATER (UNII: 059QF0KO0R)	0.9053 g  in 1 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0001 g  in 1 mL
PROPYLENE GLYCOL ALGINATE (UNII: 26CD3J2R0C)	0.1 g  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70302-063-00	100 in 1 CARTON	04/06/2020
1		1 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/06/2020

HAND SANITIZER 50 SINGLE USE VIALS X 1ML EA 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70302-065
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
KONJAC MANNAN (UNII: 36W3E5TAMG)	0.002 g  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.1 g  in 1 mL
WATER (UNII: 059QF0KO0R)	0.9053 g  in 1 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0001 g  in 1 mL
PROPYLENE GLYCOL ALGINATE (UNII: 26CD3J2R0C)	0.1 g  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70302-065-00	50 in 1 CARTON	04/06/2020
1		1 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/06/2020

Labeler - Unipharma, LLC (079524332)

Establishment
Name	Address	ID/FEI	Business Operations
Unipharma, LLC		079524332	manufacture(70302-063, 70302-065)