Instant Hand Sanitizer

Manufacturer
OP Biotech Co., Ltd.
Effective date
2020-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:19

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Apply on palm, spread and rub over back of hands and fingertips until dry. It will make your hands clean.

Storage and handling

Store in a cool and dry place. Avoid high temperature, humidity and direct sunlight. Expiration date 3 years.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For cleaning your hands to decrease bacteria on the skin that can potentially cause disease.

Warnings

WARNINGS SECTION

Highly flammable. Keep away from fire and flames. For external use only.

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occur, rinse eyes thoroughly with water.

Keep out of reach of children. Get medical help immediately if swallowed.

Stop use and ask a doctor if irritation and redness develop.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Get medical help immediately if swallowed.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply on palm, spread and rub over back of hands and fingertips until dry. It will make your hands clean.

Other information

STORAGE AND HANDLING SECTION

Store in a cool and dry place. Avoid high temperature, humidity and direct sunlight. Expiration date 3 years.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Acrylates/C-10-30 Alkyl Acrylate Copolymer, Aminomethyl Propanol, Melaleuca Alterfolia (Tea Tree) Leaf Oil

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer BoxOuter BoxInner Packet LabelInner Packet Label003 mL NDC: 75798-001-03

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75798-00175798-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
c19cae72-f401-050d-e053-2a95a90abf98a504780e-6ceb-a0f8-e053-2a95a90affde2021-05-05WarningsExact identifier
spl set id: a504780e-6ceb-a0f8-e053-2a95a90affde

Reported adverse events (FAERS/openFDA)#

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