HY-IQ HAND AND SURFACE DISINFECTANT AND SANITIZER- hy-iq water spray

Hy-IQ Hand and Surface Disinfectant and Sanitizer by

Drug Labeling and Warnings

Hy-IQ Hand and Surface Disinfectant and Sanitizer by is a Otc medication manufactured, distributed, or labeled by HAND SANITIZER LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

Hydrogen Cation .77%

PURPOSE

Antimicrobial

INDICATIONS & USAGE

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

WARNINGS

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

DOSAGE & ADMINISTRATION

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

OTHER SAFETY INFORMATION

Store under 110°F (43C)

INACTIVE INGREDIENT

Water, UREA

Hy-IQ HAND and SURFACE DISINFECTANT AND SANITIZER

Hy-IQ HAND and SURFACE DISINFECTANT AND SANITIZER

INGREDIENTS AND APPEARANCE

HY-IQ HAND AND SURFACE DISINFECTANT AND SANITIZER 
hy-iq water spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76701-362
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN CATION (UNII: 5046UKT60S) (HYDROGEN CATION - UNII:5046UKT60S)	HYDROGEN CATION	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	940 mg  in 1 mL
UREA (UNII: 8W8T17847W)	50 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76701-362-16	473.176 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2021
2	NDC: 76701-362-02	50.275 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2021
3	NDC: 76701-362-32	946.353 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2021
4	NDC: 76701-362-76	3785.41 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/17/2021

Labeler - HAND SANITIZER LLC (117473019)

Establishment
Name	Address	ID/FEI	Business Operations
HAND SANITIZER LLC		117473019	label(76701-362) , pack(76701-362) , manufacture(76701-362)