OTC Medication Information: Raon Hand Sanitizer Gel

RAON HAND SANITIZER GEL- alcohol gel
Liz Corporation Co., Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

79487-202-01
(click image for full-size original)

79487-202-02
(click image for full-size original)
RAON HAND SANITIZER GEL
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:79487-202
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 70 mg in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ALOE VERA LEAF
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
BUTYLENE GLYCOL
ARTEMISIA VULGARIS ROOT
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:79487-202-01 500 mL in 1 BOTTLE, PUMP None
2 NDC:79487-202-02 50 mL in 1 BOTTLE, PUMP None
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 Operations
Liz Corporation Co., Ltd 694803273 manufacture (79487-202)

Revised: 02/2021 Liz Corporation Co., Ltd

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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