Mint Hand Sanitizer

Manufacturer: Ni Hau Industrial Co., Ltd.
Effective date: 2022-01-06
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:18:57

Label at a glance#

ProductMint Hand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

Squeeze a small amount into your palm and briskly rub together until dry.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away for fire and flames.

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of eye contact, flush with water. Do not inhale or ingest. Keep out of reach of children. Stop Use and ask a doctor if skin irritation develops

OTC - STOP USE SECTION

Stop Use and ask a doctor if skin irritation develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Squeeze a small amount into your palm and briskly rub together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Propanediol, Polyacrylic Acid, Fragrance, Triethanolamine Cyclohexane, Limonene, Linalool.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug FactsFront Label45 mL NDC: 77189-004-45

Products#

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

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

Mint Hand Sanitizer
ALCOHOL
PROPANEDIOL
LIMONENE, (+)-
POLYACRYLIC ACID (250000 MW)
FRAGRANCE LAVENDER & CHIA F-153480
TRIETHANOLAMINE 2-CYCLOHEXYL-4,6-DINITROPHENOLATE
LINALOOL, (+)-
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77189-004	77189-004-45

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
Name	UNII	Kind
PROPANEDIOL	5965N8W85T	IACT
LIMONENE, (+)-	GFD7C86Q1W	IACT
ALCOHOL	3K9958V90M	ACTIB
POLYACRYLIC ACID (250000 MW)	9G2MAD7J6W	IACT
FRAGRANCE LAVENDER & CHIA F-153480	SXS9CO2TZK	IACT
TRIETHANOLAMINE 2-CYCLOHEXYL-4,6-DINITROPHENOLATE	N2TK31JIAH	IACT
LINALOOL, (+)-	F4VNO44C09	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f1266cd4-2986-695d-e053-2a95a90a47b2			a501f159-a904-2d1a-e053-2995a90a39fe	2022-12-31	Warnings	Exact identifier spl set id: a501f159-a904-2d1a-e053-2995a90a39fe

Reported adverse events (FAERS/openFDA)#

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