INSTANT HAND SANITIZER- alcohol gel

Instant Hand Sanitizer by

Drug Labeling and Warnings

Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by OP Biotech Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75%. Purpose: Antiseptic

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria on the skin.

Warnings

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.

WHEN USING

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.

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

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

Other information

Store below 30C (86F)

May discolor certain fabrics or surfaces

Inactive ingredients

Water, Carbomer, Aminomethyl propanol, Orange oil

Package Label - Principal Display Panel

300 mL NDC: 75798-002-30

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75798-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
CARBOMER 1342 (UNII: 809Y72KV36)
ORANGE OIL (UNII: AKN3KSD11B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75798-002-30	300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/07/2020

Labeler - OP Biotech Co., Ltd. (658280709)

Establishment
Name	Address	ID/FEI	Business Operations
OP Biotech Co., Ltd.		658280709	manufacture(75798-002)