AQ PURE INSTANT HAND SANITIZER- alcohol gel
DAY GREAT 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.

----------

AQ pure Instant Hand Sanitizer

Drug Facts

Active Ingredients

Alcohol 80%

Purpose

Antiseptic

Uses:

wet hands bacteria on the skin that could disease
recommended for repeated uses

Directions:

wet hands thoroughly with product and allow to dry without wiping
not recommende for infants

Warnings:

For external use only
Flammable
Keep away from heat and flame
Do not store above 40 degrees Celcius (15 degrees Farenheit)

Do not use

in mouth, ears or eyes

When using this product,

avoid contact with eyes
In case of contact, flush eyes with water

Stop use and seek a doctor

if redness or irritation develops and persist for more than 72 hours
Children must be supervise in use of this product
Pump as needed into your palms and thoroughly spread on both hands
Rub in to skin until dry

Keep out of reach of children

children must be supervised in the use of this product

Other Information:

may discolor some fabrics
harmful to wood finishes and plastics

Inactive Ingredients:

water
triethanolamine
acrylates/c 10-30 alkyl crosspolymer
glycerin

Package Labeling:290ml

Bottle

Package Labeling:480ml

Bottle2

AQ PURE INSTANT HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79333-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.8 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:79333-001-07	290 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/13/2020
2	NDC:79333-001-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/13/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	07/13/2020

Labeler - DAY GREAT LLC (122472915)