RAON HAND SANITIZING WIPES- benzalkonium chloride liquid

Raon Hand Sanitizing Wipes by

Drug Labeling and Warnings

Raon Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Liz Corporation Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Use

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For external use only : hands

Flammable. Keep away from heat and flame.

When using this product

• Keep out of eyes. In case of contact with eyse, flush thoroughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest.

Stop use and ask a doctor if

• irritation and redness develop skin irritation or rash develops
• condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wipe hands thoroughly with product and allow to dry
• Discard wipe in trash. Do not flush.

Inactive ingredients

Water, Glycerin, Polysorbate 80, Sodium Benzoate, Citric Acid, Maltodextrin, Aloe Barbadensis Leaf Juice Powder, Fragrance, Tocopheryl Acetate

Package Label

INGREDIENTS AND APPEARANCE

RAON HAND SANITIZING WIPES 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79487-204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79487-204-01	279 g in 1 POUCH; Type 0: Not a Combination Product	02/20/2021
2	NDC: 79487-204-02	93 g in 1 POUCH; Type 0: Not a Combination Product	02/20/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/20/2021

Labeler - Liz Corporation Co., Ltd (694803273)

Registrant - Liz Corporation Co., Ltd (694803273)

Establishment
Name	Address	ID/FEI	Business Operations
Liz Corporation Co., Ltd		694803273	manufacture(79487-204)