ALCOHOL FREE HAND SANITIZER- benzalkonium chloride liquid 
Guide Energy Solutions LLC

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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CLEANDURANCETM ALCOHOL FREE HAND SANITIZER 

Drug Facts

Active ingredient[s]

Benzalkonium Chloride 0.13%

Purpose

Skin Antiseptic

Use[s]

For hand and skin sanitizing to decrease microbes on skin.

Warnings

For external use only. Do not use in the eyes. In case of eye contact, flush thoroughly with water & seek medical attention.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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

Directions

Dispense an adequate amount in palm to cover hands.

Rub hands together to cover skin thoroughly until dry.

Supervise young children while using this product.

Other information

*Skin cells may be shed naturally or by abrasion prior to 4 hours, exposing fresh, unprotected skin. Reapply as needed.

Inactive ingredients

Water, Calcium Silicate

Kills 99.99% of Bacteria & Viruses

4-HR HAND SANITIZER

• NON-FLAMMABLE

• NON-TOXIC

• DYE FREE

• FRAGRANCE FREE

MADE IN THE USA

Manufactured By:

Guide Solutions
9330 S. Highway 99
Prague, OK 74864
405-567-0710

FDA Registered

Packaging

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ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77042-110
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CALCIUM SILICATE (UNII: S4255P4G5M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77042-110-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
2NDC:77042-110-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
3NDC:77042-110-013785 mL in 1 JUG; Type 0: Not a Combination Product08/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/01/2020
Labeler - Guide Energy Solutions LLC (117045830)

Revised: 10/2020
Document Id: 14bfaf3b-0398-47b7-8d1a-7f8952005891
Set id: 27171f80-1e8e-4a63-a61e-4fae937270b2
Version: 5
Effective Time: 20201028
 
Guide Energy Solutions LLC