XOXO Disinfectant

Manufacturer: Hand Sanitizer LLC
Effective date: 2021-09-11
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:42:27

Label at a glance#

ProductXOXO Disinfectant

Active ingredientHYDROGEN CATION

Label structure9 sections

Indications and uses

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

Dosage and administration

Spray enough XOXO Skin Disinfectant Spray to thoroughly dampen hands or hard surfaces. For hands, rub together until dry. For surfaces, wipe dry with a clean cloth, towel, or sponge.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydrogen Cation .77%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children

Directions

DOSAGE & ADMINISTRATION SECTION

Spray enough XOXO Skin Disinfectant Spray to thoroughly dampen hands or hard surfaces. For hands, rub together until dry. For surfaces, wipe dry with a clean cloth, towel, or sponge.

Other Safety Information

Store under 110º F (43º C)

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water, Urea

XOXO DISINFECTANT SPRAY

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

XOXOSkin Label 8.375x3.5 091021 16 ounce-01XOXO DISINFECTANT SPRAY

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76701-401-02	2022-07-29	C162847	48780-1	e4f33bdf-a023-d8a0-e053-dadaa90a6e4e	XOXO Disinfectant
76701-401-08	2022-07-29	C162847	48780-1	e4f33bdf-a023-d8a0-e053-dadaa90a6e4e	XOXO Disinfectant
76701-401-16	2022-07-29	C162847	48780-1	e4f33bdf-a023-d8a0-e053-dadaa90a6e4e	XOXO Disinfectant
76701-401-32	2022-07-29	C162847	48780-1	e4f33bdf-a023-d8a0-e053-dadaa90a6e4e	XOXO Disinfectant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
76701-401-02	XOXO Disinfectant	50.275 mL in 1 BOTTLE, SPRAY	SPRAY	50.275	1
76701-401-08	XOXO Disinfectant	237 mL in 1 BOTTLE, SPRAY	SPRAY	237	1
76701-401-16	XOXO Disinfectant	473.176 mL in 1 BOTTLE, SPRAY	SPRAY	473.176	1
76701-401-32	XOXO Disinfectant	946.353 mL in 1 BOTTLE, SPRAY	SPRAY	946.353	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76701-401	XOXO DISINFECTANT (HY-IQ) SPRAY [HAND SANITIZER LLC]	1	Legacy NDC, 4 package rows	20210921_cb99229a-9323-797e-e053-2995a90ac128.zip

Products#

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

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

XOXO Disinfectant
Hy-IQ
HYDROGEN CATION
UREA
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76701-401	76701-401-32, 76701-401-16, 76701-401-08, 76701-401-02

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
HYDROGEN CATION	5046UKT60S	ACTIB
UREA	8W8T17847W	IACT
WATER	059QF0KO0R	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
cb99229a-9324-797e-e053-2995a90ac128			cb99229a-9323-797e-e053-2995a90ac128	2021-09-11	Warnings	Exact identifier spl id: cb99229a-9324-797e-e053-2995a90ac128 spl set id: cb99229a-9323-797e-e053-2995a90ac128

Reported adverse events (FAERS/openFDA)#

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