GOOD TO GO SANITIZING KIT- benzalkonium chloride, alcohol kit

Good To Go Sanitizing Kit by

Drug Labeling and Warnings

Good To Go Sanitizing Kit by is a Otc medication manufactured, distributed, or labeled by Navajo Manufacturing Company Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Hand Sanitizing Wipes Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antimicrobial

Uses

• for hand sanitizing to decrease bacteria on the skin
• recommended for repeated use

Warnings

For external use only

When using this product avoid contact with eyes. In case of contact, flush eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Take wipe and rub thoroughly over all surfaces of both hands.
• Rub hands together briskly to dry.
• Dispose of wipe.

Inactive ingredients

Aloe Barbadensis Leaf Juice, Purified water (Aqua), Glycerin, Nonionic Surfactant

Hand Sanitizer Drug Facts

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

• A hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from fire or flam or sparks.

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

Stop use and ask a doctor if irritation or rash appears on the skin.

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

Directions

• Place enough to cover both hands in the palm, and rub hands together until dry.
• Children under 6 years of age should be supervised by an adult when applying this product.

Other information

• Store below 110°F (43°C).
• May discolor certain fabrics or surfaces.

Inactive ingredients

Purified water, triethanolamine, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, carbomer, aloe barbadensis leaf juice, fragrance.

Questions or comments?

Call 1-800-525-5097

Principal Display Panel

Made in China

INGREDIENTS AND APPEARANCE

GOOD TO GO SANITIZING KIT 
benzalkonium chloride, alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67751-193

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67751-193-01	1 in 1 KIT; Type 1: Convenience Kit of Co-Package	06/30/2020

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE	59 mL
Part 2		15

Part 1 of 2

HANDY SOLUTIONS INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E 
alcohol liquid

Product Information
Item Code (Source)	NDC: 67751-085
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
TROLAMINE (UNII: 9O3K93S3TK)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67751-085-03	59 mL in 1 BOTTLE; 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	part333E	10/28/2011

Part 2 of 2

HANDY SOLUTIONS ANTIBACTERIAL HAND WIPES 
benzalkonium chloride liquid

Product Information
Item Code (Source)	NDC: 67751-194
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.00013

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333a,part333e	06/30/2020

Labeler - Navajo Manufacturing Company Inc. (091917799)

Registrant - Navajo Manufacturing Company Inc. (136941411)

Establishment
Name	Address	ID/FEI	Business Operations
Navajo Manufacturing Company Inc.		136941411	manufacture(67751-193) , pack(67751-193)