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 66% v/v Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer Wipes

Use

Hand sanitizer to reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only

Flammable. Keep away from heat and flame.

WHEN USING

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

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

• Wipe hands thoroughly for approximately 30 seconds
• discard after single use
• Supervise children under 6 years of age when using this product to avoid swallowing

Other information

store between 15-40°C (59-105ºF) avoid freezing and excessive heat above 40°C (104ºF)

Inactive ingredients

water (aqua), citric acid, butylene glycol, propolis extract, fragrance (parfum)

Package Label - Principal Display Panel

NDC: 75214-401-60

LABBCIN

LABBCIN V3 ANTIBACTERIAL HAND SANITIZING WIPES

66% ALCOHOL

KILLS 99.9% GERMS

60 wipes

INGREDIENTS AND APPEARANCE

HAND SANITIZER WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75214-401
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	66 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPOLIS WAX (UNII: 6Y8XYV2NOF)	0.01 mL  in 100 mL
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	0.05 mL  in 100 mL
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	0.1 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	37.39 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75214-401-10	66.67 mL in 1 PACKAGE; Type 0: Not a Combination Product	04/28/2020
2	NDC: 75214-401-60	400 mL in 1 PACKAGE; Type 0: Not a Combination Product	04/28/2020

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(75214-401)