RICO HAND SANITIZER- alcohol cloth

Rico Hand Sanitizer by

Drug Labeling and Warnings

Rico Hand Sanitizer 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)

Alcohol 62% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

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

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, Citric Acid Monohydrate, Butylene Glycol, Propolis Extract, Fragrance

Package Label - Principal Display Panel

Rico Hand Sanitizer

50 wipes

kills 99.9% of common illness causing Germs

INGREDIENTS AND APPEARANCE

RICO HAND SANITIZER 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75214-504
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65.67 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPOLIS WAX (UNII: 6Y8XYV2NOF)	0.01 mL  in 100 mL
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	0.03 mL  in 100 mL
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	0.5 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	33.74 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75214-504-50	334 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(75214-504)