Moxe

Manufacturer: Nutrix International, LLC.
Effective date: 2020-05-11
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:10:52

Label at a glance#

ProductMoxe

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Use[s]

INDICATIONS & USAGE SECTION

Drug Facts PanelUse to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

• For external use only.

• Flammable.

• Keep away from heat 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

OTC - STOP USE SECTION

A Doctor If skin irritation develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contacta Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

• Place sanitizer on palm, rub hands together.

• Supervise children under 6 years of age.

Other Information

OTHER SAFETY INFORMATION

Do not store over 110º F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance

Purpose

OTC - PURPOSE SECTION

Antiseptic

Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CompleteLabel 4ozLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73333-011-01	2022-01-28	C162847	48780-1	d6a99b39-8b8d-a426-e053-dadaa90af4c2	a5667972-2b56-caaf-e053-2995a90ad4c2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73333-011-01	Moxe	118 g in 1 BOTTLE	GEL	118		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73333-011	MOXE (CITRUS HAND SANITIZER 4OZ) GEL [NUTRIX INTERNATIONAL, LLC.]	1	Legacy NDC, 1 package rows	20200512_a5667972-2b56-caaf-e053-2995a90ad4c2.zip

Products#

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

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

Moxe
Citrus Hand Sanitizer 4oz
TANGERINE
TROLAMINE
ALCOHOL
CARBOMER 940
PROPYLENE GLYCOL
WATER
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73333-011	73333-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TANGERINE	KH3E3096OO	IACT
TROLAMINE	9O3K93S3TK	IACT
ALCOHOL	3K9958V90M	ACTIB
CARBOMER 940	4Q93RCW27E	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT

Source Document#

Source XML · Source PDF

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
a566190f-5219-6077-e053-2a95a90a19cd			a5667972-2b56-caaf-e053-2995a90ad4c2	2020-05-11	Warnings	Exact identifier spl id: a566190f-5219-6077-e053-2a95a90a19cd spl set id: a5667972-2b56-caaf-e053-2995a90ad4c2

Reported adverse events (FAERS/openFDA)#

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