AQ pure Instant Hand Sanitizer

Manufacturer: DAY GREAT LLC
Effective date: 2020-07-31
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:23:26

Label at a glance#

ProductAQ pure Instant Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

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

Warnings:

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

in mouth, ears or eyes

When using this product,

OTC - WHEN USING SECTION

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

Stop use and seek a doctor

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

children must be supervised in the use of this product

Other Information:

SPL UNCLASSIFIED SECTION

may discolor some fabrics
harmful to wood finishes and plastics

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

water
triethanolamine
acrylates/c 10-30 alkyl crosspolymer
glycerin

Package Labeling:290ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

Package Labeling:480ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041498	ethanol 80 % Topical Gel	PSN	1
1041498	ethanol 0.8 ML/ML Topical Gel	SCD	1
1041498	ethanol 80 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79333-001-07	2022-01-28	C162847	48780-1	d6a99b39-5e9e-a426-e053-dadaa90af4c2	AQ pure Instant Hand Sanitizer
79333-001-08	2022-01-28	C162847	48780-1	d6a99b39-5e9e-a426-e053-dadaa90af4c2	AQ pure Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79333-001-07	AQ pure Instant Hand Sanitizer	290 mL in 1 BOTTLE	GEL	290		1
79333-001-08	AQ pure Instant Hand Sanitizer	480 mL in 1 BOTTLE	GEL	480		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79333-001	AQ PURE INSTANT HAND SANITIZER (ALCOHOL) GEL [DAY GREAT LLC]	1	Legacy NDC, 2 package rows	20200801_abbf4f33-4741-3024-e053-2995a90a0724.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

AQ pure Instant Hand Sanitizer
ALCOHOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
WATER
TROLAMINE
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79333-001	79333-001-07, 79333-001-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
abbf4e2c-e61c-1253-e053-2a95a90a1cb5			abbf4f33-4741-3024-e053-2995a90a0724	2020-07-31	Warnings	Exact identifier spl id: abbf4e2c-e61c-1253-e053-2a95a90a1cb5 spl set id: abbf4f33-4741-3024-e053-2995a90a0724

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.