Hand Sanitizer Wipes

Manufacturer
HANUL CO.,LTD
Effective date
2025-01-20
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 00:53:15

Label at a glance#

ProductHand Sanitizer Wipes
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

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

Ethyl Alcohol 70% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer Wipes

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

  • 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, glycerin, hydrogen peroxide

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 75214-501-50

RICO HAND SANITIZING WIPES

NON STERILE SOLUTION

70% ALCOHOL ANTISEPTIC

Decreasing bacteria on the skin that could cause disease

50 wipes

wipes dimension 6in. x 8 In (15cm x 20m)

80wipes80wipes

50wipes50wipes

20 wipes20 wipes

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN7
1489307ethanol 0.7 ML/ML Medicated PadSCD7
1489307ethanol 70 % Medicated PadSY7
1489307ethanol 70 % Medicated WipesSY7
1489307ethyl alcohol 70 % ClothSY7

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75214-501-20Hand Sanitizer Wipes134 mL in 1 PACKAGECLOTH1347
75214-501-50Hand Sanitizer Wipes334 mL in 1 PACKAGECLOTH3347
75214-501-80Hand Sanitizer Wipes534 mL in 1 PACKAGECLOTH5347

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75214-501HAND SANITIZER WIPES (ALCOHOL) CLOTH [HANUL CO.,LTD]7Current NDC, Legacy NDC, 3 package rows20250121_a3424b96-74b0-21c4-e053-2a95a90ae7ea.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75214-50175214-501-50, 75214-501-20, 75214-501-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hand Sanitizer WipesALCOHOLHANUL CO.,LTDa3424b96-74b0-21c4-e053-2a95a90ae7ea2025-01-20WarningsExact identifier
ndc (package): 75214-501-50
ndc (package): 75214-501-80
ndc (package): 75214-501-20
ndc (product): 75214-501
ndc11 (package): 75214050180
ndc11 (package): 75214050120
ndc11 (package): 75214050150
spl id: 2c28f6ab-89e9-f61e-e063-6394a90a7edc
spl set id: a3424b96-74b0-21c4-e053-2a95a90ae7ea

Reported adverse events (FAERS/openFDA)#

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