FDA.reportPublic FDA data

Pasion Instant Hand Sanitizer

Manufacturer
MING FAI ENTERPRISE INTERNATIONAL CO., LTD
Effective date
2020-04-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:33:14

Label at a glance#

ProductPasion Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• to help reduce bacteria on the skin.

Dosage and administration

• Squeeze a significant amount in your palm and rub hands until fully dry. • Rinse free.

Label contents#

Full prescribing information#

Active Ingredient 

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

  • For external use only. • Flammable.

• Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

• avoid contact with eyes.
• If contact occurs, rinse thoroughly with water.

Stop using and ask a doctor if 

OTC - STOP USE SECTION

• irritation or redness develops and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• In case of accidental ingestion, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• Squeeze a significant amount in your palm and rub hands until fully dry. • Rinse free.

Other information

SPL UNCLASSIFIED SECTION

• Store below 110°F (43°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Phenoxyethanol, Melaleuca Alternafolia (Tea Tree) Leaf Oil, Aminomethyl propanol.

Package Labeling:72135-030-50

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:72135-030-30

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:72135-030-10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74548-03074548-030-50, 74548-030-30, 74548-030-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
PHENOXYETHANOLHIE492ZZ3TIACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALCOHOL3K9958V90MACTIB

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
b8145e89-aa47-209a-e053-2995a90a1e90a3e06290-e35c-b9d1-e053-2995a90a9d372021-01-04WarningsExact identifier
spl set id: a3e06290-e35c-b9d1-e053-2995a90a9d37

Reported adverse events (FAERS/openFDA)#

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