Good to Go Sanitizing 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., Nantong Health & Beyond Hygienic Products Inc., Zhejiang Qimei Commodity Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GOOD TO GO SANITIZING KIT- benzalkonium chloride, alcohol 
Navajo Manufacturing Company Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Good to Go Sanitizing Kit

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

GTG Sanitizing Kit

GOOD TO GO SANITIZING KIT 
benzalkonium chloride, alcohol kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 67751-195
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 67751-195-011 in 1 KIT; Type 1: Convenience Kit of Co-Package06/30/2020
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 1 20 
Part 21 BOTTLE 59 mL
Part 1 of 2
ANTIBACTERIAL WET WIPES 
benzalkonium chloride swab
Product Information
Item Code (Source)NDC: 69821-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE (UNII: V5VD430YW9)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
GLYCERIN (UNII: PDC6A3C0OX)  
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2020
Part 2 of 2
HANDY SOLUTIONS INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E 
alcohol liquid
Product Information
Item Code (Source)NDC: 67751-085
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 67751-085-0359 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/28/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333a,part333e06/30/202007/02/2022
Labeler - Navajo Manufacturing Company Inc. (091917799)
Registrant - Navajo Manufacturing Company Inc. (136941411)
Establishment
NameAddressID/FEIBusiness Operations
Nantong Health & Beyond Hygienic Products Inc.421280161manufacture(67751-085)
Establishment
NameAddressID/FEIBusiness Operations
Zhejiang Qimei Commodity Co.,Ltd.544331136manufacture(69821-001)

Revised: 1/2023