Sanixusa Hand Sanitizer

Manufacturer: GUANGZHOU RAINHOME PHARM&TECH CO., LTD | Chilla Beverages USA
Effective date: 2020-05-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:14:58

Label at a glance#

ProductSanixusa Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Warnings

WARNINGS SECTION

For External Use Only. FLAMMABLE. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months of age. On open skin wounds.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor.

OTC - STOP USE SECTION

If irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing

Other Information

OTHER SAFETY INFORMATION

Store between 15-30C (59-85F).

Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, C10 30 alkyl acrylate crosspolymer, aminomethyl propanol, glycerin, aloe barbadensis (leaf) extract

Sanixusa Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 ml60 ml500 ml1L200 ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78126-110-02	2022-01-28	C162847	48780-1	d6a99b39-f40f-a426-e053-dadaa90af4c2	Sanixusa Hand Sanitizer
78126-110-03	2022-01-28	C162847	48780-1	d6a99b39-f40f-a426-e053-dadaa90af4c2	Sanixusa Hand Sanitizer
78126-110-06	2022-01-28	C162847	48780-1	d6a99b39-f40f-a426-e053-dadaa90af4c2	Sanixusa Hand Sanitizer
78126-110-16	2022-01-28	C162847	48780-1	d6a99b39-f40f-a426-e053-dadaa90af4c2	Sanixusa Hand Sanitizer
78126-110-33	2022-01-28	C162847	48780-1	d6a99b39-f40f-a426-e053-dadaa90af4c2	Sanixusa Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78126-110-02	Sanixusa Hand Sanitizer	60 mL in 1 BOTTLE	GEL	60		1
78126-110-03	Sanixusa Hand Sanitizer	100 mL in 1 BOTTLE	GEL	100		1
78126-110-06	Sanixusa Hand Sanitizer	200 mL in 1 BOTTLE	GEL	200		1
78126-110-16	Sanixusa Hand Sanitizer	500 mL in 1 BOTTLE	GEL	500		1
78126-110-33	Sanixusa Hand Sanitizer	1000 mL in 1 BOTTLE	GEL	1000		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78126-110	SANIXUSA HAND SANITIZER (ETHYL ALCOHOL 75%) GEL [GUANGZHOU RAINHOME PHARM&TECH CO., LTD]	1	Legacy NDC, 5 package rows	20200528_a698a344-d19e-6212-e053-2a95a90a2265.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Sanixusa Hand Sanitizer
Ethyl Alcohol 75%
ALCOHOL
WATER
ALOE VERA LEAF
AMINOMETHYLPROPANOL
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78126-110	78126-110-03, 78126-110-02, 78126-110-06, 78126-110-16, 78126-110-33

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)	71DD5V995L	IACT
GLYCERIN	PDC6A3C0OX	IACT

Source Document#

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
a6987ed1-722c-352d-e053-2995a90a7a4c			a698a344-d19e-6212-e053-2a95a90a2265	2020-05-26	Warnings	Exact identifier spl id: a6987ed1-722c-352d-e053-2995a90a7a4c spl set id: a698a344-d19e-6212-e053-2a95a90a2265

Reported adverse events (FAERS/openFDA)#

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