FDA.reportPublic FDA data

NURI CARE Hand Sanitizing Wipes

Manufacturer
SUNJU CORPORATION | Nuricham, Inc.
Effective date
2020-06-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:27:28

Label at a glance#

ProductNURI CARE Hand Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry Supervise children under 6 years of age when using this product

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Children under 2 years ask a doctor before use.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues 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
  • Supervise children under 6 years of age when using this product

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Hydroxide

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 Sheets NDC: 75272-002-30 20 Sheets NDC: 75272-002-3020 Sheets NDC: 75272-002-30

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75272-002-302025-12-23C16284748780-1d6a99b39-3f51-a426-e053-dadaa90af4c2a56a315a-8e14-4d48-e053-2a95a90a68ad
75272-002-302022-01-28C16284748780-1d6a99b39-3f51-a426-e053-dadaa90af4c2a56a315a-8e14-4d48-e053-2a95a90a68ad

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75272-002NURI CARE HAND SANITIZING WIPES (HAND SANITIZING WIPES) CLOTH [SUNJU CORPORATION]3Legacy NDC20200609_a56a315a-8e14-4d48-e053-2a95a90a68ad.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75272-00275272-002-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

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
46981b1e-33cd-453d-e063-6294a90a6846a56a315a-8e14-4d48-e053-2a95a90a68ad2025-12-22WarningsExact identifier
spl set id: a56a315a-8e14-4d48-e053-2a95a90a68ad

Reported adverse events (FAERS/openFDA)#

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