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 23:32:20

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Put enough of KleanCare in your palm then briskly rub your hands together until dry.

Storage and handling

Store below 30C (86F) May discolor certain fabrics or surfaces

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

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Highly flammable. Keep away from flame.

Keep out of reach of children. If swallowed contact a Poison Information Center or a doctor immediately.

External use only.

Avoid use in or near eyes. Rinse eyes with water in case of contact.

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - WHEN USING SECTION

Keep out of reach of children. If swallowed contact a Poison Information Center or a doctor immediately.

Avoid use in or near eyes. Rinse eyes with water in case of contact.

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed contact a Poison Information Center or a doctor immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough of KleanCare in your palm then briskly rub your hands together until dry.

Other information

STORAGE AND HANDLING SECTION

Store below 30C (86F)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Aminomethyl propanol, Orange oil

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels300 mL NDC: 75798-002-30

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75798-00275798-002-30

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
c19cae72-f400-050d-e053-2a95a90abf98a5073fae-1cd6-7678-e053-2995a90a05a62021-05-05WarningsExact identifier
spl set id: a5073fae-1cd6-7678-e053-2995a90a05a6

Reported adverse events (FAERS/openFDA)#

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