Rico Hand Sanitizer

Manufacturer: HANUL CO.,LTD
Effective date: 2025-01-20
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:53:16

Label at a glance#

ProductRico Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Directions Wet hands thoroughly with product and allow to dry without wiping Not recommended for infants

Storage and handling

Do not store above 105ºF/40°C May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only: Hands

Flammable. Keep away from fire and flame.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation or redness develops

condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

Wet hands thoroughly with product and allow to dry without wiping

Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105ºF/40°C

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rico Hand Sanitizer

50 wipes

kills 99.9% of common illness causing Germs

rico hand sanitizing wipes

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75214-504-50	2024-11-09	C162847	48780-1	f386c64a-1f95-0266-e053-dadaa90a7c1a	Rico Hand Sanitizer Wipes 50
75214-504-50	2023-01-30	C162847	48780-1	f386c64a-1f95-0266-e053-dadaa90a7c1a	Rico Hand Sanitizer Wipes 50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75214-504-50	Rico Hand Sanitizer	334 mL in 1 PACKAGE	CLOTH	334		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75214-504	RICO HAND SANITIZER (ALCOHOL) CLOTH [HANUL CO.,LTD]	4	Current NDC, Legacy NDC, 1 package rows	20250121_a6065fcd-3968-d5a1-e053-2a95a90ab8d6.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

Rico Hand Sanitizer
ALCOHOL
ANHYDROUS CITRIC ACID
BUTYLENE GLYCOL
WATER
PROPOLIS WAX

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75214-504	75214-504-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
WATER	059QF0KO0R	IACT
PROPOLIS WAX	6Y8XYV2NOF	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Rico Hand Sanitizer	ALCOHOL	HANUL CO.,LTD	a6065fcd-3968-d5a1-e053-2a95a90ab8d6	2025-01-20	Warnings	Exact identifier ndc (package): 75214-504-50 ndc (product): 75214-504 ndc11 (package): 75214050450 spl id: 2c290914-c825-ebe8-e063-6294a90aa3a5 spl set id: a6065fcd-3968-d5a1-e053-2a95a90ab8d6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.