FDA.reportPublic FDA data

Aerium Hand Sanitizer 70% 50ml

Manufacturer
SM Global, LLC. | E.CIS COSMETIC.Co.,Ltd
Effective date
2020-05-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:14:29

Label at a glance#

ProductAerium Hand Sanitizer 70% 50ml
Active ingredientALCOHOL
Label structure13 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 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

active ingredientactive ingredient

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

purposepurpose

Use

INDICATIONS & USAGE SECTION

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

useuse

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

warningswarnings

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds
  • do not usedo not use

When using

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.

When usingWhen using

Stop use

OTC - STOP USE SECTION

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

Stop useStop use

Keep out

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.
Keep outKeep out

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.
  • DirectionsDirections

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Aminomethyl Propanol, Mentha Arvensis Leaf Oil, Tocopheryl Acetate, Panthenol, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract

inactive ingredientsinactive ingredients

Questions or Comments?

OTC - QUESTIONS SECTION

1-800-819-4159

questionsquestions

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aerium Hand Sanitizer
Helps reduce bacteria and germs

Contains Recommended 70 % Alcohol Content
Moisturizes with Aloe Formula
Sanitizes to Help Reduce the Spread of Germs

Ethyl Alcohol 70%

50ml / 1.69 fl.oz

PDPPDP

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
74924-102-032022-01-28C16284748780-1d6a99b39-f3fd-a426-e053-dadaa90af4c2Aerium Hand Sanitizer 70% 50ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74924-102-01Aerium Hand Sanitizer 70% 50ml50 mL in 1 BOTTLEGEL502
74924-102-02Aerium Hand Sanitizer 70% 50ml12 in 1 PACKAGEGEL122
74924-102-03Aerium Hand Sanitizer 70% 50ml72 in 1 CARTONGEL722

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74924-102AERIUM HAND SANITIZER 70% 50ML (ETHYL ALCOHOL) GEL [SM GLOBAL, LLC.]2Legacy NDC, 3 package rows20200525_a5838ccf-1042-e7df-e053-2995a90a9663.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74924-10274924-102-01, 74924-102-02, 74924-102-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER 9404Q93RCW27EIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PANTHENOLWV9CM0O67ZIACT
HYALURONATE SODIUMYSE9PPT4THIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a6724c98-dcad-48b2-e053-2a95a90a8cdda5838ccf-1042-e7df-e053-2995a90a96632020-05-25WarningsExact identifier
spl id: a6724c98-dcad-48b2-e053-2a95a90a8cdd
spl set id: a5838ccf-1042-e7df-e053-2995a90a9663

Reported adverse events (FAERS/openFDA)#

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