Instant Hand Sanitizer

Manufacturer
OP Biotech Co., Ltd.
Effective date
2020-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:21

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Apply an appropriate amount of Hand Gel into palms and spread on both hands. Rub into skin until dry.

Storage and handling

Store in 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

Ethyl 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

Do not freeze. For external use only.

Do not use in ears or mouth. Highly flammable. Keep away from fire and flames.

Avoid contact with eyes. In case of contact, flush eyes with water.

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

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

OTC - WHEN USING SECTION

Do not use in ears or mouth. Highly flammable. Keep away from fire and flames.

Avoid contact with eyes. In case of contact, flush eyes with water.

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

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

OTC - STOP USE SECTION

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

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 an appropriate amount of Hand Gel into palms and spread on both hands. Rub into skin until dry.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Carbomer, Aminomethyl propanol, Orange oil

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels300 mL NDC: 75798-003-30

Products#

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DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75798-00375798-003-30

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
c19c9e46-3fab-5113-e053-2a95a90a7b63a507f54b-dad5-ec19-e053-2995a90abd8d2021-05-05WarningsExact identifier
spl set id: a507f54b-dad5-ec19-e053-2995a90abd8d

Reported adverse events (FAERS/openFDA)#

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