FDA.reportPublic FDA data

JUC RINSEFREE ANTI MICROBIAL HAND SANITIZER

Manufacturer
NMS Technologies Co., Ltd. | A03 Lab of BTS
Effective date
2020-05-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:28:16

Label at a glance#

ProductJUC RINSEFREE ANTI MICROBIAL HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Press several times, take an appropriate amount of this product to disinfect and wipe your whole hands.

Storage and handling

Storage in a cool, dry and ventilated place, sealed.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 3mg/mL. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial.

Use

INDICATIONS & USAGE SECTION

This product is indicated use to disinfection on surfaces of hands and skin to kill Escherichia coli, Staphylococcus aureus, Candida albicans.

Warnings

WARNINGS SECTION

This product should not be taken orally, and to avoid contact strong acids and bases.

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

When using: avoid direct contact with eyes and damaged skin; if it gets in your eyes accidentally, please rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

This product should be placed out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Press several times, take an appropriate amount of this product to disinfect and wipe your whole hands.

Other information

STORAGE AND HANDLING SECTION

Storage in a cool, dry and ventilated place, sealed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerol, Propylene glycol, Hydroxyethyl Cellulose, Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

S250S250

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78128-20178128-201-06

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
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT

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
299b9f2e-cacc-db98-e063-6294a90aec69a6a3db31-b456-427c-e053-2a95a90a58cf2024-12-19WarningsExact identifier
spl set id: a6a3db31-b456-427c-e053-2a95a90a58cf

Reported adverse events (FAERS/openFDA)#

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