FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Be Moxe, LLC | JW Nutritional, LLC
Effective date
2022-02-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:07

Label at a glance#

ProductMOXE Citrus 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, Fragrance

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 118 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MOXĒ

CITRUS

HAND
SANITIZER

70% Alcohol

MADE IN
USA

4FL OZ | 118ml

PRINCIPAL DISPLAY PANEL - 118 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 118 ml Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75435-813-042024-01-30C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-082024-01-30C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-122024-01-30C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-322024-01-30C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-042022-04-09C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-082022-04-09C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-122022-04-09C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-322022-04-09C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-042022-01-28C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-082022-01-28C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-122022-01-28C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer
75435-813-322022-01-28C16284748780-1d6a99b39-dc3f-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75435-813-04MOXE Citrus Hand Sanitizer118 mL in 1 BOTTLEGEL1182
75435-813-08MOXE Citrus Hand Sanitizer237 mL in 1 BOTTLEGEL2372
75435-813-12MOXE Citrus Hand Sanitizer355 mL in 1 BOTTLEGEL3552
75435-813-32MOXE Citrus Hand Sanitizer946 mL in 1 BOTTLEGEL9462

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75435-813MOXE CITRUS HAND SANITIZER (ALCOHOL) GEL [BE MOXE, LLC]2Legacy NDC, 4 package rows20220409_a0bad565-edd9-46f7-aad6-cc8998573e68.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
75435-81375435-813-04, 75435-813-08, 75435-813-12, 75435-813-32

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
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
Carbomer Homopolymer, Unspecified Type0A5MM307FCIACT
GlycerinPDC6A3C0OXIACT
AloeV5VD430YW9IACT
.Alpha.-Tocopherol Acetate9E8X80D2L0IACT

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
dfd71e4d-021e-4651-bb16-a8a0c8025730a0bad565-edd9-46f7-aad6-cc8998573e682022-02-08WarningsExact identifier
spl id: dfd71e4d-021e-4651-bb16-a8a0c8025730
spl set id: a0bad565-edd9-46f7-aad6-cc8998573e68

Reported adverse events (FAERS/openFDA)#

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