HAND SANITIZER WIPES- alcohol cloth

Hand Sanitizer Wipes by

Drug Labeling and Warnings

Hand Sanitizer Wipes by is a Otc medication manufactured, distributed, or labeled by HANUL CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75% Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer Wipes

Use

To decrease bacteria on the skin that could cause disease

Warnings

For external use only: hands

Flammable. Keep away from fire and flame.

WHEN USING

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

avoid contact with broken skin

do not inhale or ingest

STOP USE

Stop Use and ask a doctor if

irritation or redness develops

condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands thoroughly with product and allow to dry without wiping
• Not recommended for infants

Other information

do not store above 105ºF/40°C

may discolor some fabrics

harmful to wood finishes and plastics

Inactive ingredients

water, glycerin, hydrogen peroxide

Package Label - Principal Display Panel

rico

hand sanitizer wipes

non-sterile solution

kills 99.9 of common illness-causing germs

75% alcohol antiseptic

INGREDIENTS AND APPEARANCE

HAND SANITIZER WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75214-503
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
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75214-503-50	334 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 75214-503-10	134 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 75214-503-80	534 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - HANUL CO.,LTD (557814370)

Establishment
Name	Address	ID/FEI	Business Operations
HANUL CO.,LTD		557814370	manufacture(75214-503)