Hi-IQ Hand Sanitizer

Manufacturer: Hand Sanitizer LLC
Effective date: 2021-06-29
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:41:08

Label at a glance#

ProductHi-IQ Hand Sanitizer

Active ingredientHYDROGEN CATION

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Hy- IQ Water ( [H9O4] | [H5O2] )

Hydrogen Cation .77%

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

For spraying on hands or hard surfaces in order to prevent the spreading of bacteria & harmful germs.

WARNINGS SECTION

For external use only. Do not use if you are allergi to any ingredients. Stop use if rash develops and ask a doctor right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children

DOSAGE & ADMINISTRATION SECTION

Spray liberally on hard surfaces or hands. Allow to either dry naturally by air, or by drying with a clean paper towel, fabic towel, or sponge.

OTHER SAFETY INFORMATION

Store under 110°F (43C)

INACTIVE INGREDIENT SECTION

Water, UREA

Hy-IQ Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hy - IQ Hand Sanitizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76701-350-01	2022-07-29	C162847	48780-1	e4f33bdf-9d3e-d8a0-e053-dadaa90a6e4e	c50ca22c-1893-a257-e053-2995a90ad37f
76701-350-16	2022-07-29	C162847	48780-1	e4f33bdf-9d3e-d8a0-e053-dadaa90a6e4e	c50ca22c-1893-a257-e053-2995a90ad37f
76701-350-28	2022-07-29	C162847	48780-1	e4f33bdf-9d3e-d8a0-e053-dadaa90a6e4e	c50ca22c-1893-a257-e053-2995a90ad37f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
76701-350-01	Hi-IQ Hand Sanitizer	50.275 mL in 1 BOTTLE, PUMP	SPRAY	50.275	3
76701-350-16	Hi-IQ Hand Sanitizer	473.176 mL in 1 BOTTLE, SPRAY	SPRAY	473.176	3
76701-350-28	Hi-IQ Hand Sanitizer	3785.41 mL in 1 BOTTLE	SPRAY	3785.41	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76701-350	HI-IQ HAND SANITIZER (HI-IQ WATER) SPRAY [HAND SANITIZER LLC]	3	Legacy NDC, 3 package rows	20210630_c50ca22c-1893-a257-e053-2995a90ad37f.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Hi-IQ Hand Sanitizer
Hi-IQ Water
WATER
HYDROGEN CATION
UREA

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76701-350	76701-350-01, 76701-350-16, 76701-350-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
HYDROGEN CATION	5046UKT60S	ACTIB
UREA	8W8T17847W	IACT

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
c5efade7-98e6-2cfa-e053-2995a90a6923			c50ca22c-1893-a257-e053-2995a90ad37f	2021-06-29	Warnings	Exact identifier spl id: c5efade7-98e6-2cfa-e053-2995a90a6923 spl set id: c50ca22c-1893-a257-e053-2995a90ad37f

Reported adverse events (FAERS/openFDA)#

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