Moxe

Manufacturer: Nutrix International, LLC.
Effective date: 2020-06-19
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:18:26

Label at a glance#

ProductMoxe

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

• Place sanitizer on palm, rub hands together. • Supervise children under 6.

Contacts and useful links#

PhoneLabel contact1-800-296-3160

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol w/w 70%

Use

INDICATIONS & USAGE SECTION

Use to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

• For external use only.

• Flammable.

• Keep away from fire or flame.

Do Not Use

OTC - DO NOT USE SECTION

Do Not Use Near Eyes. In case of contact, rinse eyes thoroughly with water

Stop Use And Ask A Doctor

OTC - STOP USE SECTION

If skin irritation develops.

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 sanitizer on palm, rub hands together.

• Supervise children under 6.

Other Information

OTHER SAFETY INFORMATION

Do not store over 110º F

Questions?

OTC - QUESTIONS SECTION

Call 1-800-296-3160

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Acrylates Copolymer, TEA, Glycerin, Propylene Glycol, Fragrance.

Purpose

OTC - PURPOSE SECTION

LabelAntiseptic

Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelDrug FactsFront Label

Drug Fact

Complete Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73333-340-01	2022-01-28	C162847	48780-1	d6a99b39-a9aa-a426-e053-dadaa90af4c2	a8748fe6-1259-7314-e053-2995a90a1902

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73333-340-01	Moxe	340 g in 1 BOTTLE	LOTION	340		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73333-340	MOXE (CITRUS HAND SANITIZER 12OZ) LOTION [NUTRIX INTERNATIONAL, LLC.]	1	Legacy NDC, 1 package rows	20200620_a8748fe6-1259-7314-e053-2995a90a1902.zip

Products#

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

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

Moxe
Citrus Hand Sanitizer 12oz
CARBOMER 940
TANGERINE
GLYCERIN
WATER
ALCOHOL
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73333-340	73333-340-01

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
CARBOMER 940	4Q93RCW27E	IACT
TANGERINE	KH3E3096OO	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
TROLAMINE	9O3K93S3TK	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
a8746486-5acb-9556-e053-2995a90a4ee8			a8748fe6-1259-7314-e053-2995a90a1902	2020-06-19	Warnings	Exact identifier spl id: a8746486-5acb-9556-e053-2995a90a4ee8 spl set id: a8748fe6-1259-7314-e053-2995a90a1902

Reported adverse events (FAERS/openFDA)#

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