ALCOHOL FREE HAND SANITIZER- benzalkonium chloride liquid

Alcohol Free Hand Sanitizer by

Drug Labeling and Warnings

Alcohol Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Guide Energy Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77042-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CALCIUM SILICATE (UNII: S4255P4G5M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77042-110-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020
2	NDC: 77042-110-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020
3	NDC: 77042-110-01	3785 mL in 1 JUG; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/01/2020

Labeler - Guide Energy Solutions LLC (117045830)