MOXE Unscented Hand Sanitizer

Manufacturer
Be Moxe, LLC | JW Nutritional, LLC
Effective date
2020-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:43

Label at a glance#

ProductMOXE Unscented Hand Sanitizer
Active ingredientAlcohol
Label structure11 sections

Indications and uses

Use to help reduce bacteria on the skin.

Dosage and administration

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

Storage and handling

Do not store over 110° F

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% by volume

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

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.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children.

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

STORAGE AND HANDLING SECTION

Do not store over 110° F

Questions?

OTC - QUESTIONS SECTION

Call 1-800-296-3160

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Aloe Leaf Juice, Tocopheryl Acetate (Vitamin E)

SPL UNCLASSIFIED SECTION

Distributed by:
Be MOXĒ LLC 4700 140th Ave N., Ste 112,
Clearwater, FL 33762

PRINCIPAL DISPLAY PANEL - 237 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MOXĒ

UNSCENTED

HAND
SANITIZER

70% Alcohol

MADE IN
USA

8FL OZ | 237ml

PRINCIPAL DISPLAY PANEL - 237 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 237 ml Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75435-002-082022-01-28C16284748780-1d6a99b39-c684-a426-e053-dadaa90af4c2MOXĒ Unscented Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75435-002-08MOXE Unscented Hand Sanitizer237 mL in 1 BOTTLEGEL2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75435-002MOXE UNSCENTED HAND SANITIZER (ALCOHOL) GEL [BE MOXE, LLC]1Legacy NDC, 1 package rows20200805_8910037d-cad7-4f97-96d3-9338705bda0e.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75435-00275435-002-08

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a792ba3b-dc2d-4918-b879-f654f22c5d6d8910037d-cad7-4f97-96d3-9338705bda0e2020-08-03WarningsExact identifier
spl id: a792ba3b-dc2d-4918-b879-f654f22c5d6d
spl set id: 8910037d-cad7-4f97-96d3-9338705bda0e

Reported adverse events (FAERS/openFDA)#

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