MOISTURIZING HAND SANITIZER

Manufacturer: RHaus II, LLC
Effective date: 2020-06-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:18:55

Label at a glance#

ProductMOISTURIZING HAND SANITIZER

Active ingredientALCOHOL

Label structure10 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 ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

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 fire or flame.

Do not use

OTC - DO NOT USE SECTION

On 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 thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and seek a doctor 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 (59-86F).
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Aloe Barbadensis Leaf Juice, Triethanolamine, Iodopropynyl Butylcarbamate, Methylisothiazolinone.

Questions?

OTC - QUESTIONS SECTION

email Info@Rhaus2.com

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTI-DIS PRO

Moisturizing Hand Sanitizer

Unscented Gel

70% Ethyl Alcohol

not today,

germs.

not today.

16.9 fl.oz 500ml

sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79181-001-01	2022-01-28	C162847	48780-1	d6a99b39-7568-a426-e053-dadaa90af4c2	RHaus Moisturizing Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79181-001-01	MOISTURIZING HAND SANITIZER	500 mL in 1 BOTTLE, PLASTIC	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79181-001	MOISTURIZING HAND SANITIZER (ALCOHOL) GEL [RHAUS II, LLC]	1	Legacy NDC, 1 package rows	20200625_a8c1e513-d2e5-2342-e053-2a95a90aa504.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

MOISTURIZING HAND SANITIZER
ALCOHOL
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
METHYLISOTHIAZOLINONE
IODOPROPYNYL BUTYLCARBAMATE
TROLAMINE
WATER
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79181-001	79181-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
IODOPROPYNYL BUTYLCARBAMATE	603P14DHEB	IACT
TROLAMINE	9O3K93S3TK	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	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
a8c1e507-e969-1a13-e053-2a95a90a7b0a			a8c1e513-d2e5-2342-e053-2a95a90aa504	2020-06-23	Warnings	Exact identifier spl id: a8c1e507-e969-1a13-e053-2a95a90a7b0a spl set id: a8c1e513-d2e5-2342-e053-2a95a90aa504

Reported adverse events (FAERS/openFDA)#

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