RAON HAND SANITIZER GEL- alcohol gel

Raon Hand Sanitizer Gel by

Drug Labeling and Warnings

Raon Hand Sanitizer Gel 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

Ethyl Alcohol 70.0%

Purpose

ANTISEPTIC

Use

Hand sanitizer to decrease bacteria on the skin that could cause disease

Warnings

For external use only. Flammable. Keep away from heat and flame.

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 and ask a doctor if

skin irritation or rash develops.

Keep out of reach of children

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

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry

Superevise children under 6 years of age when using this product to avoid swalloing.

Other information

Store between 15-30ºC (59-86ºF)

Avoid Freezing and excessive heat above 40ºC (104ºF)

Inactive ingredients

Water, Butylene Glycol, Carbomer, Triethanplamine, Aloe Barbadensis Leaf Extract, Artemisia Vulgaris Extract

Package Label

INGREDIENTS AND APPEARANCE

RAON HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79487-202
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79487-202-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/23/2021
2	NDC: 79487-202-02	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/23/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/23/2021

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(79487-202)