FDA.reportPublic FDA data

Malie Organics Mango Nectar Sanitizer

Manufacturer
Malie Organics
Effective date
2021-05-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:45:21

Label at a glance#

ProductMalie Organics Mango Nectar Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

Pour onto hands, wetting throughly with product. Rub into skin until dry. Children under 6 years of age should be supervised by an adult when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Organic Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

avoid contact with face, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pour onto hands, wetting throughly with product. Rub into skin until dry.
  • Children under 6 years of age should be supervised by an adult when using this product.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified Water (Aqua), Lavandula Angustifolia Oil*, Propanediol, Aloe Barbadensis Leaf Juice*, Fragrance, Hydroxyethylcellulose, Isopropyl Myristate, AminoMethyl Propanol.* Organic

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73731-00273731-002-01

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
WATER059QF0KO0RIACT
LAVENDER OILZBP1YXW0H8IACT
PROPANEDIOL5965N8W85TIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
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
0a21d620-da9a-2bb5-e063-6294a90ae8f8b0ecb4a5-3b58-0985-e053-2a95a90a8eca2023-11-14WarningsExact identifier
spl set id: b0ecb4a5-3b58-0985-e053-2a95a90a8eca

Reported adverse events (FAERS/openFDA)#

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