Nano Silver Cleanser Hand Sanitizer

Manufacturer
DDUnion, Co.,Ltd
Effective date
2020-10-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:31:44

Label at a glance#

ProductNano Silver Cleanser Hand Sanitizer
Active ingredientSILVER CATION, ALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

SILVER CATION,ALCOHOL

USE

INDICATIONS & USAGE SECTION

Nano Silver Cleanser Hand sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

If you are new to the product, apply it on a small area and test

to see if there is anything wrong with your skin

WHEN USING

OTC - WHEN USING SECTION

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

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Don't put it on your face

Hand sterilization and cleaning are possible, but they are

not medicines

Do not use

OTC - DO NOT USE SECTION

● in children less than 2 months of age

● on open skin wounds

Do not use in areas with abnormalities such as wound, eczema,

and dermatitis

Stop use and ask doctor

OTC - STOP USE SECTION

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

If you experience any of the following problems, do not use this product and contact your dermatologist, etc

In case of abnormalities such as red spots, swelling,

itching, irritation, etc. during use

PURPOSE

OTC - PURPOSE SECTION

Antimicrobial

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Direction

DOSAGE & ADMINISTRATION SECTION

● Spray 2~3 time on the hand or general objects exposed to contamination and then dry with

a tissue or dry cloth after 1 minute. Sprinkle 30cm below the face.

● Supervise children under 6 years of age when using this product to avoid swallowing

Other information

OTHER SAFETY INFORMATION

●Store between 15-30C (59-86F)

●Avoid freezing and excessive heat above 40C (104F)

●Year of manufacture:notation of separate diagram

●Expiration day:3years from manufacturing date

●Questions or Comments? please call 82-10-5327-9670

Inactive ingredients

INACTIVE INGREDIENT SECTION

cypress oil, poiyoxyethylene sorbitan monolaurate, purified water

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79702-301-01 50ML

79702-301-0179702-301-0179702-301-02 70ML

79702-301-0279702-301-02

79702-301-03 100ML

79702-301-0379702-301-03

79702-301-04 200ML

79702-301-0479702-301-04

79702-301-05 500ML

79702-301-0579702-301-05

79702-301-06 1000ML

79702-301-0679702-301-06

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79702-301-01Nano Silver Cleanser Hand Sanitizer50 mL in 1 BOTTLE, SPRAYSPRAY504
79702-301-02Nano Silver Cleanser Hand Sanitizer70 mL in 1 BOTTLE, SPRAYSPRAY704
79702-301-03Nano Silver Cleanser Hand Sanitizer100 mL in 1 BOTTLE, SPRAYSPRAY1004
79702-301-04Nano Silver Cleanser Hand Sanitizer200 mL in 1 BOTTLE, SPRAYSPRAY2004
79702-301-05Nano Silver Cleanser Hand Sanitizer500 mL in 1 BOTTLE, SPRAYSPRAY5004
79702-301-06Nano Silver Cleanser Hand Sanitizer1000 mL in 1 BOTTLE, SPRAYSPRAY10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79702-301NANO SILVER CLEANSER HAND SANITIZER (SILVER CATION,ALCOHOL) SPRAY [DDUNION, CO.,LTD]4Legacy NDC, 6 package rows20201016_b1c14edc-fc1a-92f4-e053-2a95a90add35.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79702-30179702-301-01, 79702-301-02, 79702-301-03, 79702-301-04, 79702-301-05, 79702-301-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b1c14edc-fc1b-92f4-e053-2a95a90add35b1c14edc-fc1a-92f4-e053-2a95a90add352020-10-15WarningsExact identifier
spl id: b1c14edc-fc1b-92f4-e053-2a95a90add35
spl set id: b1c14edc-fc1a-92f4-e053-2a95a90add35

Reported adverse events (FAERS/openFDA)#

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