FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Be Moxe, LLC
Effective date
2022-04-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:04

Label at a glance#

ProductHAND SANITIZER
Active ingredientAlcohol
Label structure10 sections

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.

Storage and handling

Store between 59-86°F (15-30°C) Avoid freezing and excessive heat above 104°F (40°C)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use[s]

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 heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 years of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 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

STORAGE AND HANDLING SECTION

  • Store between 59-86°F (15-30°C)
  • Avoid freezing and excessive heat above 104°F (40°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Isopropyl Myristate, Carbomer, Triethanolamine.

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

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 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
75435-727-082024-01-30C16284748780-1d6a99b39-c099-a426-e053-dadaa90af4c2HAND SANITIZER
75435-727-102024-01-30C16284748780-1d6a99b39-c099-a426-e053-dadaa90af4c2HAND SANITIZER
75435-727-082022-04-05C16284748780-1d6a99b39-c099-a426-e053-dadaa90af4c2HAND SANITIZER
75435-727-102022-04-05C16284748780-1d6a99b39-c099-a426-e053-dadaa90af4c2HAND SANITIZER
75435-727-082022-01-28C16284748780-1d6a99b39-c099-a426-e053-dadaa90af4c2HAND SANITIZER
75435-727-102022-01-28C16284748780-1d6a99b39-c099-a426-e053-dadaa90af4c2HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75435-727-08HAND SANITIZER237 mL in 1 BOTTLEGEL2372
75435-727-10HAND SANITIZER295 mL in 1 BOTTLEGEL2952

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75435-727HAND SANITIZER (ALCOHOL) GEL [BE MOXE, LLC]2Legacy NDC, 2 package rows20220406_bf036779-13f6-4f33-973b-3ed084e36c6b.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75435-72775435-727-08, 75435-727-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT

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
ce77e582-d1d5-4a0e-a18f-5240577272abbf036779-13f6-4f33-973b-3ed084e36c6b2022-04-05WarningsExact identifier
spl id: ce77e582-d1d5-4a0e-a18f-5240577272ab
spl set id: bf036779-13f6-4f33-973b-3ed084e36c6b

Reported adverse events (FAERS/openFDA)#

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