FDA.reportPublic FDA data

Aerium Sanitizer Spray 75% 500ml

Manufacturer
SM Global, LLC. | E.CIS COSMETIC.Co.,Ltd
Effective date
2020-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:06

Label at a glance#

ProductAerium Sanitizer 75% 500ml
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Spray 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

Alcohol 80% v/v. Purpose: Antiseptic

Active Ingredient(s)Active Ingredient(s)

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

PurposePurpose

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

UseUse

Warnings

WARNINGS SECTION

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

WarningWarning

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 this product

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 using this productWhen using this product

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Stop use and ask a doctorStop use and ask a doctor

Keep out of reach of children.

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 out of reach of childrenKeep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray 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, Fragrance(Parfum), PEG-40 Hydrogenated Castor Oil, PEG-60 Hydrogenated Castor Oil, Scutellaria Baicalensis Root Extract, Portulaca Oleracea Extract, Aloe Barbadensis Leaf Extract

Inactive IngredientsInactive Ingredients

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aerium
Sanitizer Spray
Helps reduce bacteria and germs

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

500ml/ 16.9 fl.oz.

Package Label - Principal Display PanelPackage Label - Principal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74924-110-022022-01-28C16284748780-1d6a99b39-5953-a426-e053-dadaa90af4c2Aerium Sanitizer Spray 75% 500ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74924-110-01Aerium Sanitizer 75% 500ml500 mL in 1 BOTTLESPRAY5001
74924-110-02Aerium Sanitizer 75% 500ml24 in 1 CARTONSPRAY241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74924-110AERIUM SANITIZER 75% 500ML (ETHYL ALCOHOL) SPRAY [SM GLOBAL, LLC.]1Legacy NDC, 2 package rows20200611_a7501d3a-bb99-016a-e053-2995a90a0ebe.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74924-11074924-110-01, 74924-110-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEG-60 HYDROGENATED CASTOR OIL02NG325BQGIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
PURSLANEM6S840WXG5IACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
a7500a72-3e73-08be-e053-2a95a90a1377a7501d3a-bb99-016a-e053-2995a90a0ebe2020-06-05WarningsExact identifier
spl id: a7500a72-3e73-08be-e053-2a95a90a1377
spl set id: a7501d3a-bb99-016a-e053-2995a90a0ebe

Reported adverse events (FAERS/openFDA)#

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